UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q

(Mark One)

☒ QUARTERLY REPORT PURSUANT TO SECTION 13 or 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934.

For the quarterly period ended June 30, 2025

☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934.

For the transition period from ____________ to ____________

Commission File Number 001-34471

CHINA PHARMA HOLDINGS, INC.

(Exact name of registrant as specified in its charter)

Nevada		75-1564807
(State or other jurisdiction of		(IRS Employer
incorporation or organization)		Identification No.)

Second Floor, No. 17, Jinpan Road Haikou, Hainan Province, China		570216
(Address of principal executive offices)		(Zip Code)

+86-898-6681-1730 (China)

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class		Trading Symbol(s)		Name of each exchange on which registered
Common Stock		CPHI		NYSE American

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes ☒ No ☐

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer”, “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large accelerated filer ☐	Accelerated filer ☐
Non-accelerated filer ☒	Smaller reporting company ☒
	Emerging growth company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒

As of August 7, 2025, there were 3,262,002 shares of common stock, $0.01 par value per share, issued and outstanding.

CHINA PHARMA HOLDINGS, INC. AND SUBSIDIARIES

TABLE OF CONTENTS

		Page

PART I FINANCIAL INFORMATION		1

Item 1.	Financial Statements	1

Item 2.	Management’s Discussion and Analysis of Financial Condition and Results of Operations	15

Item 3.	Quantitative and Qualitative Disclosures about Market Risk	23

Item 4.	Controls and Procedures	23

PART II OTHER INFORMATION		24

Item 6.	Exhibits	26

PART I – FINANCIAL INFORMATION

Item 1. Financial Statements

CHINA PHARMA HOLDINGS, INC. AND SUBSIDIARIES

TABLE OF CONTENTS

Condensed Consolidated Balance Sheets as of June 30, 2025 and December 31, 2024 (Unaudited)	2

Condensed Consolidated Statements of Operations and Comprehensive Loss for the Six Months Ended June 30, 2025 and 2024 (Unaudited)	3

Condensed Consolidated Statements of Stockholders’ Equity for the Six Months Ended June 30, 2025 and 2024 (Unaudited)	4

Condensed Consolidated Statements of Cash Flows for the Six Months Ended June 30, 2025 and 2024 (Unaudited)	5

Notes to Condensed Consolidated Financial Statements (Unaudited)	6

CHINA PHARMA HOLDINGS, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(Unaudited)

	June 30,			December 31,
	2025			2024
ASSETS
Current Assets:
Cash and cash equivalents	$	625,032		$	626,879
Banker’s acceptances		-			18,642
Trade accounts receivable, less allowance for credit losses of $13,644,006 and $13,587,182, respectively		268,793			232,140
Other receivables, less allowance for credit losses of $29,014 and $28,447, respectively		48,361			30,286
Advances to suppliers		4,967			14,960
Inventories		1,678,769			2,266,154
Prepaid expenses		74,869			81,328
Total Current Assets		2,700,791			3,270,389

Property, plant and equipment, net		4,625,907			4,883,401
Right-of-use assets		-			38,298
Intangible assets, net		6,439,862			6,695,436
TOTAL ASSETS	$	13,766,560		$	14,887,524

LIABILITIES AND STOCKHOLDERS’ EQUITY
Current Liabilities:
Trade accounts payable	$	530,729		$	225,106
Accrued expenses		191,293			247,159
Other payables		2,344,882			2,182,982
Contract liabilities		77,683			162,208
Borrowings from related parties		1,407,607			1,144,985
Lease liabilities		-			39,323
Current portion of lines of credit		698,461			1,015,525
Total Current Liabilities		5,250,655			5,017,288
Non-current Liabilities:
Lines of credit, net of current portion		1,319,915			1,391,130
Deferred tax liability		734,246			731,202
Total Liabilities		7,304,816			7,139,620
Commitments and Contingencies (Note 13)
Stockholders’ Equity:
Preferred stock, $0.001 par value; 5,000,000 shares authorized; no shares issued or outstanding		-			-
Common stock, $0.001 par value; 500,000,000 shares authorized; 3,262,022 shares and 3,261,911 shares issued and outstanding, respectively		3,262			3,262
Additional paid-in capital		40,631,679			40,631,679
Subscription receivable		(180,000	)		(180,000	)
Accumulated deficit		(45,340,618	)		(44,026,679	)
Accumulated other comprehensive income		11,347,421			11,319,642
Total Stockholders’ Equity		6,461,744			7,747,904
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY	$	13,766,560		$	14,887,524

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

CHINA PHARMA HOLDINGS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

AND COMPREHENSIVE LOSS

(Unaudited)

	For the Three Months						For the Six Months
	Ended June 30,						Ended June 30,
	2025			2024			2025			2024
Revenue	$	1,025,767		$	924,943		$	2,162,054		$	2,294,782
Cost of revenue		1,112,777			1,940,329			2,385,125			3,600,192

Gross loss		(87,010	)		(1,015,386	)		(223,071	)		(1,305,410	)

Operating expenses:
Selling expenses		101,292			111,455			188,403			219,642
General and administrative expenses		440,834			91,870			948,016			580,326
Research and development expenses		20,952			164,334			50,539			195,785
Credit losses		2,032			8,476			709			6,410
Total operating expenses		565,110			376,135			1,187,667			1,002,163

Loss from operations		(652,120	)		(1,391,521	)		(1,410,738	)		(2,307,573	)

Other income (expense):
Research and development subsidy		150,690			-			150,690			-
Interest income		422			1,531			1,496			3,846
Interest expense		(27,359	)		(48,140	)		(55,387	)		(90,295	)
Net other income (expense)		123,753	)		(46,609	)		96,799	)		(86,449	)

Loss before income taxes		(528,367	)		(1,438,130	)		(1,313,939	)		(2,394,022	)
Income tax expense		-			-			-			-
Net loss		(528,367	)		(1,438,130	)		(1,313,939	)		(2,394,022	)
Other comprehensive income (loss) - foreign currency translation adjustment		20,263			(45,502	)		27,778			(67,077	)
Comprehensive loss	$	(508,104	)	$	(1,483,632	)	$	(1,286,161	)	$	(2,461,099	)
Loss per share:
Basic and diluted	$	(0.16	)	$	(0.89	)	$	(0.40	)	$	(1.63	)
Weighted average shares outstanding		3,262,002			1,612,426			3,262,002			1,472,743

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

CHINA PHARMA HOLDINGS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

(Unaudited)

										Accumulated
					Additional					Other			Total
	Common Stock				Paid-in		Accumulated			Comprehensive			Stockholders’
	Shares		Amount		Capital		Deficit			Income			Equity
Balance as of December 31, 2023		1,062,579	$	1,063	$	35,291,818	$	(39,290,314	)	$	11,452,054		$	7,454,621
Conversions of Note Payable to common stock		119,109		119		449,881		-			-			450,000
Issuance of common stock for intangible assets		300,000		300		1,364,700		-			-			1,365,000
Net loss for the period		-		-		-		(955,892	)		-			(955,892	)
Foreign currency translation adjustment		-		-		-		-			(21,575	)		(21,575	)
Balance as of March 31, 2024		1,481,688		1,482		37,106,399		(40,246,206	)		11,430,479			8,292,154
Conversions of Note Payable to common stock		234,592		235		599,765		-			-			600,000
Net loss for the period		-		-		-		(1,438,130	)		-			(1,438,130	)
Foreign currency translation adjustment		-		-		-		-			(45,502	)		(45,502	)
Balance, as of June 30, 2024		1,716,280	$	1,717	$	37,706,164	$	(41,684,336	)	$	11,384,977		$	7,408,522

							Securities
					Additional		Purchase						Other		Total
	Common Stock				Paid-in		Agreement			Accumulated			Comprehensive		Stockholders’
	Shares		Amount		Capital		Receivable			Deficit			Income		Equity
Balance as of December 31, 2024	3,261,911	$	3,262	$	40,631,679		(180,000	)	$	(44,026,679	)	$	11,319,642	$	7,747,904
Net loss for the period	-		-		-		-			(785,572	)		-		(785,572	)
Foreign currency translation adjustment	-		-		-		-			-			7,516		7,516
Balance, March 31, 2025	3,261,911		3,262		40,631,679		(180,000	)		(44,812,251	)		11,327,158		6,969,848
Net loss for the period	-		-				-			(528,367	)		-		(528,367	)
Share rounding due to reverse split	91		*		-		-			-			-		-
Foreign currency translation adjustment	-		-		-		-			-			20,263		20,263
Balance, June 30, 2025	3,262,002	$	3,262		40,631,679	$	(180,000	)	$	(45,340,618	)	$	11,347,421	$	6,461,744

Less than 1.

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

CHINA PHARMA HOLDINGS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

	For the Six Months
	Ended June 30,
	2025			2024
Cash Flows from Operating Activities:
Net loss	$	(1,313,939	)	$	(2,394,022	)
Depreciation and amortization		650,176			1,473,050
Credit losses		709			6,410
Inventory write off		422,932			411,431
Changes in assets and liabilities:
Trade accounts and other receivables		(185,236	)		182,533
Advances to suppliers		10,020			1,845
Inventories		321,431			719,121
Trade accounts payable		303,613			(821,907	)
Other payables and accrued expenses		101,678			(241,434	)
Advances from customers		(84,899	)		11,142
Prepaid expenses		6,773			(6,053	)
Net Cash Provided by (Used in) Operating Activities		233,258			(657,884	)

Cash Flows from Investing Activities:
Purchases of property and equipment		(58,259	)		(28,086	)
Advances for intangible assets		(32,627	)		-
Net Cash Used in Investing Activities		(90,886	)		(28,086	)

Cash Flows from Financing Activities:
Payments of line of credit		(1,092,893	)		(492,761	)
Proceeds from lines of credit		695,999			492,761
Borrowings and interest from related party		297,673			13,708
Net Cash (Used In) Provided By Financing Activities		(99,221	)		13,708

Effect of Exchange Rate Changes on Cash		(44,998	)		(12,239	)
Net Decrease in Cash and Cash Equivalents		(1,847	)		(684,501	)
Cash and Cash Equivalents at Beginning of Period		626,879			1,423,838
Cash and Cash Equivalents at End of Period	$	625,032		$	739,337

Supplemental Cash Flow Information:
Cash paid for income taxes	$	-		$	-
Cash paid for interest	$	41,829		$	43,217

Supplemental Noncash Investing and Financing Activities:
Conversions of Note Payable to common stock		-		$	1,050,000
Issuances of stock for intangible assets		-		$	1,365,000

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

NOTE 1 – ORGANIZATION AND SIGNIFICANT ACCOUNTING POLICIES

Organization and Nature of Operations – China Pharma Holdings, Inc., a Nevada corporation (“China Pharma”), owns 100% of Onny Investment Limited (“Onny”), a British Virgin Islands corporation, which owns 100% of Hainan Helpson Medical & Biotechnology Co., Ltd (“Helpson”), a company organized under the laws of the People’s Republic of China (the “PRC”). China Pharma Holdings, Inc. and its subsidiaries are referred to herein as the Company.

Onny acquired 100% of the ownership in Helpson on May 25, 2005, by entering into an Equity Transfer Agreement with Helpson’s three former shareholders. The transaction was approved by the Commercial Bureau of Hainan Province on June 12, 2005 and Helpson received the Certificate of Approval for Establishment of Enterprises with Foreign Investment in the PRC on the same day. Helpson received its business license evidencing its Wholly Foreign Owned Enterprise (“WFOE”) status on June 21, 2005.

Helpson is principally engaged in the development, manufacture and marketing of pharmaceutical products for human use in connection with a variety of high-incidence and high-mortality diseases and medical conditions prevalent in the PRC. All of its operations are conducted in the PRC, where its manufacturing facilities are located. Helpson manufactures pharmaceutical products in the form of dry powder injectables, liquid injectables, tablets, capsules, and cephalosporin oral solutions. The majority of its pharmaceutical products are sold on a prescription basis and all have been approved for at least one or more therapeutic indications by the National Medical Products Administration (the “NMPA”, formerly China Food and Drug Administration, or CFDA) based upon demonstrated safety and efficacy.

Liquidity and Going Concern

As of June 30, 2025, the Company had cash and cash equivalents of $0.6 million and an accumulated deficit of $45.3 million and the Company’s current liabilities exceeded current assets by $2.5 million. In addition, the Company had incurred net losses of $1.3 million and had cash inflows from operating activities of $0.23 million for the six months ended June 30, 2025. The Company’s Chairperson, Chief Executive Officer and Interim Chief Financial Officer Ms. Li has advanced an additional $0.24 million during the second quarter of 2025 for an aggregate of $1,407,607 as of June 30, 2025 to provide working capital and enabled the Company to make the required payments related to its former construction loan facility and current lines of credit. The Company anticipates operating losses to continue for the foreseeable future due to, among other things, costs related to the production of its existing products, debt service costs and selling and administrative costs. These conditions raise substantial doubt about its ability to continue as a going concern within one year after the date that the financial statements are issued. To alleviate the conditions that raise substantial doubt about the Company’s ability to continue as a going concern, management plans to enhance the sales model of advance payment, and further strengthen its collection of accounts receivable. Further, the Company is currently exploring strategic alternatives to accelerate the launch of nutrition products. In addition, management believes that the Company’s existing property, plant and equipment can serve as collateral to support additional bank loans. The Company will implement multiple measures simultaneously across procurement, production, human resources, and marketing to reduce operating costs. In procurement, the Company will consolidate purchasing activities where practical to enhance bargaining power with suppliers. In production, operations will be optimized through approaches such as centralized manufacturing cycles and shifting energy-intensive processes to off-peak hours to reduce power costs. Production personnel will be deployed efficiently to minimize labor expenses while maintaining quality standards. In human resources, the Company will optimize staffing levels and implement targeted incentives to improve work efficiency and output quality, thereby controlling labor costs. Marketing expenditures will be focused on high-return channels through data-driven targeting and channel optimization. Additionally, the Company will enhance employee training in production techniques and cost management principles, fostering a culture of cost awareness throughout the organization. Management believes that, if successfully implemented, these measures may improve the Company’s cash position and allow the Company to fund its operations in the next twelve months, however, there can be no assurance that the Company will be able to fully execute the planned initiatives, achieve its strategic alternatives, and resolve the conditions raising substantial doubt about its ability to continue as a going concern.

Pursuant to the requirements of Accounting Standards Codification (ASC) 205-40, Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern management must evaluate whether there are conditions or events, considered in the aggregate, that raise substantial doubt about the Company’s ability to continue as a going concern within one year after the date that the financial statements are issued. This evaluation initially does not take into consideration the potential mitigating effect of management’s plans that have not been fully implemented as of the date the financial statements are issued. When substantial doubt exists under this methodology, management evaluates whether the mitigating effect of its plans sufficiently alleviates substantial doubt about the Company’s ability to continue as a going concern. The mitigating effect of management’s plans, however, is only considered if both (1) it is probable that the plans will be effectively implemented within one year after the date that the financial statements are issued, and (2) it is probable that the plans, when implemented, will mitigate the relevant conditions or events that raise substantial doubt about the entity’s ability to continue as a going concern within one year after the date that the financial statements are issued.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

Under ASC 205-40, the strategic alternatives being pursued by the Company cannot be considered probable at this time because none of the Company’s current plans have been finalized at the time of the issuance of these financial statements and the implementation of any such plan is not probable of being effectively implemented as none of the plans are entirely within the Company’s control. Accordingly, substantial doubt is deemed to exist about the Company’s ability to continue as a going concern within one year after the date these financial statements are issued.

The accompanying unaudited condensed consolidated financial statements have been prepared on a going concern basis, which contemplates the realization of assets and satisfaction of liabilities in the ordinary course of business. The financial statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities that might result from the outcome of the uncertainties described above.

Reverse Stock Split – Effective April 15, 2025, China Pharma implemented a 1-for -10 reverse stock split as more fully discussed in Note 12. All share and per share disclosures have been retroactively restated to reflect the impact of the reverse stock split.

Consolidation and Basis of Presentation – The accompanying unaudited interim condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America (“U.S. GAAP”) and are expressed in United States dollars. The accompanying unaudited interim condensed consolidated financial statements include the accounts and operations of the Company and its wholly-owned subsidiaries. All significant intercompany balances and transactions have been eliminated in the consolidation.

Helpson’s functional currency is the Chinese Renminbi. Helpson’s revenue and expenses are translated into United States dollars at the average exchange rate for the period. Assets and liabilities are translated at the exchange rate as of the end of the reporting period. Gains or losses from translating Helpson’s financial statements are included in accumulated other comprehensive income, which is a component of stockholders’ equity. Gains and losses arising from transactions denominated in a currency other than the functional currency of the entity that is party to the transaction are included in the results of operations.

In the opinion of management, the unaudited interim condensed consolidated financial statements reflect all adjustments of a normal recurring nature that are necessary for a fair presentation of the results for the interim periods presented. All significant intercompany transactions and balances are eliminated on consolidation. However, the results of operations included in such financial statements may not necessary be indicative of annual results. Such financial statements should be read in conjunction with the Company’s audited consolidated financial statements and notes thereto included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2024 filed with the Securities and Exchange Commission (the “SEC”) on March 31, 2025 (“2024 Annual Report”).

Accounting Estimates - The methodology used to prepare the Company’s financial statements is in conformity with U.S. GAAP, which requires the management of the Company to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosures of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenues and expenses during the reporting periods. Therefore, actual results could differ from those estimates.

The Company uses the same accounting policies in preparing its quarterly and annual financial statements. Certain information and footnote disclosures normally included in the annual consolidated financial statements prepared in accordance with U.S. GAAP have been condensed or omitted.

Loss Per Share - Basic loss per share is calculated by dividing loss available to common stockholders by the weighted-average number of shares of common stock outstanding, excluding unvested stock. Diluted loss per share is computed similar to basic loss per share except that the denominator is increased to include the number of additional shares of common stock that would have been outstanding if the potential common shares, including unvested stock, had been issued and if the additional common shares were dilutive.

The potentially dilutive common shares related to the option to purchase 1,330 shares of common stock as of June 30, 2025 and 2024 are excluded from the computation of diluted net loss per share for all periods presented because the effect is anti-dilutive due to net losses of the Company.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

Recent Accounting Pronouncements

In November 2024, the FASB issued ASU 2024-03, “Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses”. The amendments in this ASU are intended to improve financial reporting by requiring that public business entities disclose additional information about specific expense categories in the notes to financial statements at interim and annual reporting periods. For interim and annual reporting periods, an entity shall disaggregate, in a tabular format disclosure in the notes to financial statements, all relevant expense captions presented on the face of the income statement in continuing operations into the purchases of inventory, employee compensation, depreciation, amortization, and depletion. This ASU is effective for annual reporting periods beginning after December 15, 2026, and interim reporting periods beginning after December 15, 2027. Early adoption is permitted. The amendments in this Update should be applied either (1) prospectively to financial statements issued for reporting periods after the effective date of this Update or (2) retrospectively to any or all prior periods presented in the financial statements. In January 2025, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2025-01 — Income Statement — Reporting Comprehensive Income — Expense Disaggregation Disclosures (Subtopic 220-40): Clarifying the Effective Date. This ASU amends the effective date of Update 2024-03 to clarify that all public business entities are required to adopt the guidance in annual reporting periods beginning after December 15, 2026, and interim periods within annual reporting periods beginning after December 15, 2027. We are currently evaluating the impact the adoption of ASU 2024-03 will have on its consolidated financial statements and related disclosures. We do not expect the adoption of this accounting standard to have an impact on our Consolidated Financial Statements but will require certain additional disclosures.

In November 2024, the FASB issued ASU 2024-04, Debt—Debt with Conversion and Other Options (Subtopic 470-20): Induced Conversions of Convertible Debt Instruments. The ASU provides additional guidance on whether induced conversion or extinguishment accounting should be applied to certain settlements of convertible debt instruments that do not occur in accordance with the instruments’ preexisting terms. The ASU requires entities to apply a preexisting contract approach. To qualify for induced conversion accounting under this approach, the inducement offer is required to preserve the form of consideration and result in an amount of consideration that is no less than that issuable pursuant to the preexisting conversion privileges. ASU 2024-04 clarifies how entities should assess the form and amount of consideration when applying this approach. In addition, the new ASU clarifies that induced conversion accounting can be applied to settlements of certain convertible debt instruments that are not currently convertible as long as the instrument contained a substantive conversion feature as of both its issuance date and the inducement offer acceptance date. The amendments in the ASU are effective for annual reporting periods beginning after December 15, 2025, and interim reporting periods within those annual reporting periods. Early adoption is permitted. We are currently evaluating the impact the adoption of ASU 2024-04 will have on its consolidated financial statements and related disclosures.

In January 2025, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2025-01 — Income Statement — Reporting Comprehensive Income — Expense Disaggregation Disclosures (Subtopic 220-40): Clarifying the Effective Date. This ASU amends the effective date of Update 2024-03 to clarify that all public business entities are required to adopt the guidance in annual reporting periods beginning after December 15, 2026, and interim periods within annual reporting periods beginning after December 15, 2027. Early adoption is permitted. We are currently evaluating the impact the adoption of ASU 2025-01 will have on its consolidated financial statements and related disclosures.

From time to time, the FASB or other standards setting bodies issue new accounting pronouncements. Updates to the FASB ASC are communicated through issuance of ASUs. Unless otherwise discussed, the Company believes that the recently issued guidance, whether adopted or to be adopted in the future, is not expected to have a material impact on its consolidated financial statements upon adoption.

NOTE 2 – ACCOUNTS RECEIVABLE, NET

Accounts receivable, net, consist of the following:

	June 30,			December 31,
	2025			2024
Trade accounts receivable		13,912,799			13,819,322
Less: allowance for credit loss		(13,644,006	)		(13,587,182	)
Trade accounts receivable, net	$	268,793		$	232,140

Our allowance for credit losses estimate practice using the current expected credit loss method is that we consider accounts receivable balances aged within 180 days current, except for any individual uncollectible account assessed by management. We account for the following respective percentage as bad debt allowance based on age of the accounts receivables: 10% of accounts receivable that are between 180 days and 365 days old, 70% of accounts receivable that are between 365 days and 720 days old, and 100% of accounts receivable that are greater than 720 days old.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

We recognize credit losses per actual write-offs as well as changes of allowance for credit losses. To the extent that our current allowance for credit losses is higher than that of the previous period, we recognize a credit loss for the difference during the current period, and when the current credit losses are lower than that of the previous period, we recognize a gain from the reversal of the allowance for credit losses for the difference. The allowance for credit losses balances were $13.64 million and $13.59 million as of June 30, 2025 and December 31, 2024, respectively. The changes in the allowances for credit losses during the three and six months ended June 30, 2025 and 2024 were as follows:

	For the Three Months					For the Six Months
	Ended June 30,					Ended June 30,
	2025		2024			2025		2024
Balance, Beginning of Period		13,605,157		13,759,993			13,587,182		13,786,074
Credit losses		2,032		8,476			709		6,410
Foreign currency translation adjustment		36,817		(62,392	)		56,115		(86,407	)
Balance, End of Period		13,644,006		13,706,077			13,644,006		13,706,077

NOTE 3 – INVENTORIES

Inventories consisted of the following:

	June 30,			December 31,
	2025			2024
Raw materials	$	852,032		$	880,571
Work in process		287,491			340,404
Finished goods		1,540,134			1,619,250
Total Inventories		2,679,657			2,840,225
Less: Provision for obsolescence		(1,000,888	)		(574,071	)
	$	1,678,769		$	2,266,154

Changes to the provision for obsolescence consisted of the following:

	For the Three Months					For the Six Months
	Ended June 30,					Ended June 30,
	2025		2024			2025		2024
At the beginning of the period	$	788,197	$	255,593			574,071		129,420
Charges to provision		209,553		285,173			422,932		411,431
Exchange rate		3,138		(59,584	)		3,885		(59,669	)
At the end of the period	$	1,000,888	$	481,182			1,000,888		481,182

NOTE 4 – PROPERTY, PLANT AND EQUIPMENT

Property, plant and equipment consisted of the following:

	June 30,			December 31,
	2025			2024
Permit of land use	$	393,467		$	391,836
Building		9,136,923			9,099,045
Plant, machinery and equipment		27,004,192			26,835,227
Motor vehicle		393,270			265,255
Office equipment		266,360			390,434
Total		37,194,212			36,981,797
Less: accumulated depreciation		(32,568,305	)		(32,098,396	)
Property, plant and equipment, net	$	4,625,907		$	4,883,401

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

Depreciation is computed on a straight-line basis over the estimated useful lives of the assets as follows:

Asset			Life - years
Permit of land use			40 - 70
Building			20 - 49
Plant, machinery and equipment			5 - 10
Motor vehicle			5 - 10
Office equipment			3 - 5

Depreciation relating to office equipment was included in general and administrative expenses, while all other depreciation was included in cost of revenue. Depreciation expense was $163,503 and $636,721 for the three months ended June 30, 2025 and 2024, respectively and $335,104 and $1,270,981 for the six months ended June 30, 2025 and 2024, respectively.

NOTE 5 – INTANGIBLE ASSETS

Intangible assets represent the cost of medical formulas approved for production by the NMPA, the intellectual property acquired from Chengdu Bonier Medical Technology Development Co., Ltd. through certain Technology Transfer Agreement (“Bonier Agreement”) and the invention patents and intellectual property acquired pursuant to Technology Transfer Agreements in 2024 and 2023. No costs were reclassified from advances to intangible assets during the six months ended June 30, 2025 and 2024, respectively.

There were no service fees or profit payments paid related to the Bonier Agreement or the Technology Transfer Agreements from 2024 and 2023 for the six months ended June 30, 2025 and 2024, respectively.

Approved medical formulas are amortized from the date NMPA approval is obtained over their individually identifiable estimated useful life, which range from ten to thirteen years. It is at least reasonably possible that a change in the estimated useful lives of the medical formulas could occur in the near term due to changes in the demand for the drugs and medicines produced from these medical formulas. Amortization expense relating to intangible assets was $157,360 and $104,922 for the three months ended June 30, 2025 and 2024, respectively and $315,072 and $202,069 for the six months ended June 30, 2025 and 2024 which was included in the general and administrative expenses. Medical formulas typically do not have a residual value at the end of their amortization period.

Intangible assets consisted of NMPA approved medical formulas, a Utility Model Patent and two Invention Patents as follows:

	June 30,			December 31,
	2025			2024
NMPA approved medical formulas	$	4,715,816		$	4,696,267
Technology from Bonier		1,708,192			1,701,110
Invention Patents		5,331,030			5,308,930
		11,755,038			11,706,307
Accumulated amortization		(5,599,918	)		(5,261,827	)
Net carrying amount		6,155,120			6,444,480
Intangible assets in process		284,742			250,956
	$	6,439,862		$	6,695,436

NOTE 6 – OTHER PAYABLES

Other Payables consisted of the following:

	June 30,		December 31,
	2025		2024
Compensation payable to officer	$	1,603,506	$	1,587,506
Business taxes and other		741,376		595,476
Total Other Payables	$	2,344,882	$	2,182,982

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

NOTE 7 – RELATED PARTY TRANSACTIONS

The Company had previously received advances from its Chairperson Li. Total amounts owed to her were $1,407,607 and $1,144,985 and are recorded as “Borrowings from related parties” on the accompanying condensed consolidated balance sheets as of June 30, 2025 and December 31, 2024, respectively. Chairperson Li has advanced an additional $0.24 million during the second quarter of 2025 to provide working capital and enabled the Company to make the required payments related to its current lines of credit. On July 8, 2019 the Company entered into a loan agreement in exchange for cash of RMB 4,770,000 ($738,379) with its Chairperson Li. The loan bears interest at a rate of 4.35% and was payable within one year of the loan agreement. The due date of the loan agreement has been extended annually on identical terms, and is currently due July 9, 2026. Total interest expense related to the loan for the three months ended June 30, 2025 and 2024 was $6,779 and $6,852, respectively. Total interest expense related to the loan for the six months ended June 30, 2025 and 2024 was $13,558 and $13,708, respectively. Compensation payable to the Chairperson Li is included in “Other payables” in the accompanying condensed consolidated balance sheet totaling $1,567,506 and $1,559,506 as of June 30, 2025 and December 31, 2024, respectively.

NOTE 8 – LINES OF CREDIT

On December 21, 2022 the Company entered into a new line of credit for an aggregate amount of RMB 7,300,000 (approximately $1.0 million) with interest payable monthly at a rate of 3.9% with Bank of Communications. The Company received an advance on the line of credit in the amount of RMB 3,800,000 (approximately $0.56 million) on December 30, 2022. On February 24, 2023 the Company received an advance on the line in the amount of RMB 3,500,000 (approximately $0.51 million). The Company has no further availability on this line of credit. The line of credit was paid in full on December 15, 2023, five days before the due date of December 20, 2023. On December 20, 2023, the Company received a new line of credit in the amount of RMB 3,800,000 and an interest rate of 3.9% and is due December 15, 2024. The loan was fully paid on November 7, 2024. The loan was renewed on identical terms and an advance was made in the amount of RMB3,800,000 on November 11, 2024 with the balance maturing on June 21, 2025. On December 2, 2024 the Company repaid the RMB 3,500,000 and renewed the line on identical terms. The RMB 3,500,000 was advance on the same date, with the due date of the loan maturing on June 21, 2025. On June 17, 2025, the Company repaid the loan balance of RMB 7,300,000 (approximately $1.0 million). On June 25, 2025 the Company obtained a new line of credit facility in the amount of RMB 5,000,000 and received proceeds of RMB 5,000,000 (approximately $0.7 million). The new facility has an interest rate of 3.6%. The loan is due on June 20, 2026. In addition, the Company’s Chief Executive Officer and Chair of the Board personally guaranteed the new line of credit and pledged personal assets as collateral for the loan. Total interest expense under this facility for the three months ended June 30, 2025 and 2024 was $9,687 and $10,237, respectively, and $19,606 and $19,302 for the six months ended June 30, 2025 and 2024, respectively.

On September 25, 2023 the Company entered into a three-year revolving loan and received proceeds of RMB 10,000,000 (approximately $1.4 million). The interest rate for the loan is 3.35% for the first twelve months of the loan and adjusts based on the latest one-year loan market quotation rate less 10 basis points as published by the China National Interbank Funding Center on the working day prior to each twelve month anniversary of the loan. With the reduction of the Loan Prime Rate by the bank on September 20, 2024, the loan interest rate for this transaction was lowered to 3.25% effective September 21, 2024. Additionally, the company repaid RMB 551,250 (approximately $76,500) through June 30, 2025. The loan is due on September 24, 2026. The loan is collateralized by the Company’s new production facility and the included production line equipment and machinery. In addition, the Company’s Chief Executive Officer and Chair of the Board personally guaranteed the new line of credit. Total interest paid on this loan was $10,924 and $11,993 for the three months ended June 30, 2025 and 2024, respectively, and $22,247 and $23,915 for the six months ended June 30, 2025 and 2024, respectively.

Principal payments required for the remaining terms of the loan facility and lines of credit as of June 30, 2025 are as follows:

Year	Lines of Credit
2025		698,461
2026		1,319,915
	$	2,018,376

Fair Value of Lines of Credit – Based on the borrowing rates currently available to the Company for bank loans with similar terms and maturities, the carrying amounts of the lines of credit outstanding as of June 30, 2025 and December 31, 2024 approximated their fair values because the underlying instruments bear an interest rate that approximates current market rates.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

NOTE 9 – LEASES

The Company has leases for certain office and production facilities in the PRC which are classified as operating leases. The leases contain payment terms for fixed amounts. Options to extend are recognized as part of the lease liabilities and recognized as right of use assets when management estimates to renew the lease. There are no residual value guarantees, no variable lease payments, and no restrictions or covenants imposed by leases. The discount rate used in measuring the lease liabilities and right of use assets was determined by reviewing the Company’s incremental borrowing rate at the initial measurement date. For the three months ended June 30, 2025 and 2024, operating lease cost was $19,291 and $19,228, respectively and cash paid for amounts included in the measurement of lease liabilities for operating cash flows from operating leases was $20,013 and $20,142, respectively. For the six months ended June 30, 2025 and 2024, operating lease cost was $38,468 and $38,629, respectively and cash paid for amounts included in the measurement of lease liabilities for operating cash flows from operating leases was $39,906 and $40,074, respectively. As of June 30, 2025 and December 31, 2024, the Company reported right of use assets of $0 and $38,298, respectively and lease liabilities of $0 and $39,323, respectively. As of June 30, 2025, the Company no longer has any remaining operating leases.

The Company has leases with terms less than one year for certain provincial sales offices that are not material.

NOTE 10 – INCOME TAXES

Deferred income tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which temporary differences are expected to be recovered or settled. The effect of a change in tax laws or rates on deferred tax assets and liabilities is recognized in income in the period that includes the enactment date.

Liabilities are established for uncertain tax positions expected to be taken in income tax returns when such positions are judged to meet the “more-likely-than-not” threshold based on the technical merits of the positions. Estimated interest and penalties related to uncertain tax positions are included as a component of other expenses. Through December 31, 2024, the Company has not identified any uncertain tax positions that it has taken. U.S. income tax returns for the years ended December 31, 2020 through December 31, 2024 and the Chinese income tax return for the year ended December 31, 2024 are open for possible examination.

Under the current tax law in the PRC, the Company is and will be subject to the enterprise income tax rate of 25%.

There was no provision for income taxes for the three and six months ended June 30, 2025 and 2024, respectively due to continued net losses of the Company.

As of June 30, 2025, Helpson had net operating loss carryforwards for PRC tax purposes of approximately $22.1 million which are available to offset any future taxable income through 2030. Approximately $6.7 million of these carryforwards will expire in December 2025. The Company also has net operating losses for United States federal income tax purposes of approximately $11.1 million of which $5.1 million is available to offset future taxable income, if any, through 2040, and $6.0 million are available for carryforward indefinitely subject to a limitation of 80% of taxable income for each tax year.

On July 4, 2025, the One Big Beautiful Bill Act (“OBBBA”) was enacted in the U.S. The OBBBA includes significant provisions, such as the permanent extension of certain expiring provisions of the Tax Cuts and Jobs Act, modifications to the international tax framework and the restoration of favorable tax treatment for certain business provisions. The Company is currently assessing its impact on our condensed consolidated financial statements. U.S. federal tax legislation, commonly referred to as the Tax Cuts and Jobs Act (the “U.S. Tax Reform”), was signed into law on December 22, 2017. The U.S. Tax Reform significantly modified the U.S. Internal Revenue Code by, among other things, reducing the statutory U.S. federal corporate income tax rate from 35% to 21% for taxable years beginning after December 31, 2017; limiting and/or eliminating many business deductions; migrating the U.S. to a territorial tax system with a one-time transition tax on a mandatory deemed repatriation of previously deferred foreign earnings of certain foreign subsidiaries; subject to certain limitations, generally eliminating U.S. corporate income tax on dividends from foreign subsidiaries; and providing for new taxes on certain foreign earnings.

In assessing the realizability of deferred tax assets, management considers whether it is more likely than not that some portion or all of the deferred tax assets will not be realized. The ultimate realization of deferred tax assets is dependent upon the generation of future taxable income during the periods in which those differences become deductible or tax loss carry forwards are utilized. Management considers projected future taxable income and tax planning strategies in making this assessment. Based upon an assessment of the level of historical taxable income and projections for future taxable income over the periods on which the deferred tax assets are deductible or can be utilized, management believes it is not likely for the Company to realize all benefits of the deferred tax assets as of June 30, 2025 and December 31, 2024. Therefore, the Company provided for a valuation allowance against its deferred tax assets of $22,100,657 and $21,702,958 as of June 30, 2025 and December 31, 2024, respectively.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

The Company also incurred various other taxes, comprised primarily of business taxes, value-added taxes, urban construction taxes, education surcharges and others. Any unpaid amounts are reflected on the balance sheets as accrued taxes payable.

NOTE 11 – FAIR VALUE MEASUREMENTS

Fair value is defined as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. To measure fair value, a hierarchy has been established which requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs. This hierarchy uses three levels of inputs to measure the fair value of assets and liabilities as follows: Level 1 – Quoted prices in active markets for identical assets or liabilities; Level 2 – Observable inputs other than Level 1 including quoted prices for similar assets or liabilities, quoted prices in less active markets, or other observable inputs that can be corroborated by observable market data; and Level 3 – Unobservable inputs supported by little or no market activity for financial instruments whose value is determined using pricing models, discounted cash flow methodologies, or similar techniques, as well as instruments for which the determination of fair value requires significant management judgment or estimation.

The Company uses fair value to measure the value of the banker’s acceptance notes it holds at June 30, 2025 and December 31, 2024. The banker’s acceptance notes are recorded at cost which approximates fair value. The Company held the following assets and liabilities recorded at fair value:

			Fair Value Measurements at
	June 30,		Reporting Date Using
Description	2025		Level 1		Level 2		Level 3
Banker’s acceptance notes	$	-	$	-	$	-	$	-
Total	$	-	$	-	$	-	$	-

		December 31,		Fair Value Measurements at Reporting Date Using
Description		2024		Level 1		Level 2		Level 3
Banker’s acceptance notes	$	18,642	$	-	$	18,642	$	-
Total	$	18,642	$	-	$	18,642	$	-

NOTE 12 – STOCKHOLDERS’ EQUITY

China Pharma is authorized to issue 500,000,000 shares of common stock, $0.001 par value, and 5,000,000 shares of preferred stock, $0.001 par value. The preferred stock may be issued in series with such designations, preferences, stated values, rights, qualifications or limitations as determined solely by the Board of China Pharma.

According to relevant PRC laws, companies registered in the PRC, including China Pharma’s PRC subsidiary, Helpson, are required to allocate at least 10% of their after tax income, as determined under the accounting standards and regulations in the PRC, to statutory surplus reserve accounts until the reserve account balances reach 50% of the company’s registered capital prior to their remittance of funds out of the PRC. Allocations to these reserves and funds can only be used for specific purposes and are not transferrable to the parent company in the form of loans, advances or cash dividends. The amount designated for general and statutory capital reserves is $8,145,000 at June 30, 2025 and December 31, 2024.

Effective April 15, 2025, the Company implemented a 1-for-10 reverse split of its common stock. The reverse stock split was approved by the Company’s Board of Directors through unanimous written consent and the Company’s stockholders at its Annual Meeting for the fiscal year ended on December 31, 2023, which was held on December 22, 2024. Upon the effectiveness of the reverse stock split, every 10 shares of the Company’s issued and outstanding common stock were automatically converted into one share of issued and outstanding common stock. No fractional shares were issued as a result of the reverse stock split. Instead, any fractional shares that resulted from the split were rounded up to the next whole number. The reverse stock split affects all stockholders uniformly and does not alter any stockholder’s percentage interest in the Company’s outstanding common stock, except for adjustments that may result from the treatment of fractional shares. All share and per share amounts have been retroactively restated for all periods presented in the accompanying unaudited condensed consolidated financial statements.

CHINA PHARMA HOLDINGS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SIX MONTHS ENDED JUNE 30, 2025 AND 2024 (UNAUDITED)

Effective March 6, 2024, the Company implemented a 1-for-5 reverse split of its common stock. The reverse stock split was approved by the Company’s Board of Directors through unanimous written consent and the Company’s stockholders at its Annual Meeting for the fiscal year ended on December 31, 2022, which was held on December 17, 2023. Upon the effectiveness of the reverse stock split, every 5 shares of the Company’s issued and outstanding common stock were automatically converted into one share of issued and outstanding common stock. No fractional shares were issued as a result of the reverse stock split. Instead, any fractional shares that resulted from the split were rounded up to the next whole number. The reverse stock split affects all stockholders uniformly and does not alter any stockholder’s percentage interest in the Company’s outstanding common stock, except for adjustments that may result from the treatment of fractional shares. All share and per share amounts have been retroactively restated for all periods presented in the accompanying consolidated financial statements.

2010 Incentive Plan

On November 12, 2010, the Company’s Board adopted the Company’s 2010 Incentive Plan (the “Plan”), which was then approved by stockholders on December 22, 2010. On October 17, 2019, the Board of Directors approved the First Amendment to the 2010 Incentive Plan (the “Amendment”), pursuant to which the term of the 2010 Incentive Plan was extended to December 31, 2029. The Amendment was adopted by the stockholders on December 19, 2019. On October 25, 2021, the Board of Directors approved, and on December 27, 2021 our stockholders adopted the Amendment No.2 to the Plan to increase the number of shares of the Common Stock, that are reserved thereunder by 10,000 shares from 8,000 shares to 18,000 shares. On October 27, 2022 the Board of Directors approved and on December 27, 2022, the stockholders adopted the Amended and Restated Long Term 2010 Incentive Plan to increase the number of shares of common stock that are reserved thereunder by an additional 10,000 shares from 18,000 to 28,000. On December 17, 2023 the stockholders approved Amendment No. 1 to the Amended and Restated Long Term 2010 Incentive Plan to increase the number of shares from 28,000 to 58,000. On December 22, 2024 the stockholders approved Amendment No. 2 to the Amended and Restated Long Term 2010 Incentive Plan to increase the number of shares from 58,000 to 69,600. The Plan gives the Company the ability to grant stock options, restricted stock, stock appreciation rights and performance units to its employees, directors and consultants, or those who will become employees, directors and consultants of the Company and/or its subsidiaries. The Plan currently allows for equity awards of up to 69,600 shares of common stock. Through June 30, 2025, there were 8,470 shares of stock and stock options granted and outstanding under the Plan. A total of 1,330 options were outstanding as of June 30, 2025 under the Plan. As such, there are 59,800 additional units available for issuance under the Plan.

There were no issuances of securities from the Plan for the sixmonths ended June 30, 2025 and as such, no compensation expense was recognized for the period.

As of June 30, 2025, there was no remaining unrecognized compensation expense related to stock options or restricted stock grants.

NOTE 13 – COMMITMENTS AND CONTINGENCIES

Current vulnerability due to certain concentrations

For the six months ended June 30, 2025, one customer accounted for 11.5% of sales and two customers accounted for 63.5% and 13.7% of accounts receivable. Three suppliers accounted for 24.9%, 19.4% and 16.4% of raw material purchases, and three different products accounted for 32.8%, 22.8% and 13.5% of revenue.

For the six months ended June 30, 2024, no customer accounted for greater than 10.0% of sales and two customers accounted for 63.6% and 13.7% of accounts receivable. Three suppliers accounted for 23.5%, 23.4% and 17.6% of raw material purchases, and three different products accounted for 35.2%, 22.7% and 10.2% of revenue.

Nature of Operations

Economic environment - Substantially all of the Company’s operations are conducted in the PRC, and therefore the Company is subject to special considerations and significant risks not typically associated with companies operating in the United States of America. These risks include, among others, the political, economic and legal environments and fluctuations in the foreign currency exchange rate. The Company’s results from operations may be adversely affected by changes in the political and social conditions in the PRC, and by changes in governmental policies with respect to laws and regulations, anti-inflationary measures, currency conversion and remittance abroad, and rates and methods of taxation, among other things. The unfavorable changes in global macroeconomic factors may also adversely affect the Company’s operations.

In addition, all of the Company’s revenue is denominated in the PRC’s currency of Renminbi (RMB), which must be converted into other currencies before remittance out of the PRC. Both the conversion of RMB into foreign currencies and the remittance of foreign currencies abroad require approval of the PRC government.

NOTE 14 – SUBSEQUENT EVENTS

The Company evaluates all events and transactions that occur after June 30, 2025 up through the date the Company issues these condensed consolidated financial statements. There is no other subsequent event occurred that would require recognition or disclosure in the Company’s condensed consolidated financial statements.

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

The statements contained in this report with respect to our financial condition, results of operations and business that are not historical facts are forward-looking statements. Forward-looking statements can be identified by the use of forward-looking terminology, such as “anticipate,” “believe,” “expect,” “plan,” “intend,” “seek,” “estimate,” “project,” “could,” or the negative thereof or other variations thereon, or by discussions of strategy that involve risks and uncertainties. Management wishes to caution the readers that any such forward-looking statements contained in this report reflect our current beliefs with respect to future events and involve known and unknown risks, uncertainties and other factors, including, but not limited to, economic, competitive, regulatory, technological, key employees, and general business factors affecting our operations, markets, growth, services, products, licenses and other factors, some of which are described in this report and some of which are discussed in our other filings with the Securities and Exchange Commission (the “SEC”). These forward-looking statements are only estimates or predictions. No assurances can be given regarding the achievement of future results, as actual results may differ materially as a result of risks facing our company, and actual events may differ from the assumptions underlying the statements that have been made regarding anticipated events.

These risk factors should be considered in connection with any subsequent written or oral forward-looking statements that we or persons acting on our behalf may issue. All written and oral forward-looking statements made in connection with this report that are attributable to our company or persons acting on our behalf are expressly qualified in their entirety by these cautionary statements. Given these uncertainties, we caution investors not to unduly rely on our forward-looking statements. We do not undertake any obligation to review or confirm analysts’ expectations or estimates or to release publicly any revisions to any forward-looking statements to reflect events or circumstances after the date of this report or to reflect the occurrence of unanticipated events, except as required by applicable law or regulation.

Business Overview & Recent Developments

China Pharma Holding Inc. (“China Pharma”) is not a Chinese operating company but a Nevada holding company. All of our operations are conducted in the PRC through Hainan Helpson Medical & Biotechnology Co., Ltd (“Helpson”), our wholly owned subsidiary incorporated under the laws of the People’s Republic of China (the “PRC”), where the manufacturing facilities are located. Helpson is principally engaged in the development, manufacture and marketing of pharmaceutical products for human use in connection with a variety of high-incidence and high-mortality diseases and medical conditions prevalent in the PRC. It manufactures pharmaceutical products in the form of dry powder injectables, liquid injectables, tablets, capsules, and cephalosporin oral solutions. The majority of its pharmaceutical products are sold on a prescription basis and all of them have been approved for at least one or more therapeutic indications by the National Medical Products Administration (the “NMPA”, formerly China Food and Drug Administration, or CFDA) based upon demonstrated safety and efficacy.

China’s consistency evaluation of generic drugs continues to proceed for the three months ended June 30, 2025. Helpson has always taken the task of promoting the consistency evaluation as a top priority, and worked on them actively. However, for each drug’s consistency evaluation, due to the continuous dynamic changes of the detailed consistency evaluation policies, market trends, expected investments, and expected returns of investment (“ROI”), the whole industry, including Helpson, has been making slow progresses in terms of the consistency evaluation. One of the flagship products, Candesartan tablets, a hypertension product, has passed generic-drug-consistency-evaluation in early August 2023.

Helpson has taken a more cautious and flexible attitude towards initiating and progressing any project for existing products’ consistency evaluation to cope with the changing macro environment of drug sales in China. In 2018, relevant Chinese authorities decided to implement trial Centralized Procurement (“CP”) activities in 11 selected pilot cities (including 4 municipalities and 7 other cities), since then, ten rounds of CP activities have been carried out as of August 7, 2025, which significantly reduced the price of the drugs that won the bids. In addition, the consistency evaluation has been adopted as one of the qualification standards for participating in the CP activities. As a result, Helpson needs to balance between the market access brought by CP, the investment of financial resources and time to obtain the qualification of CP, and the sharp decline in the price of drugs included in CP before making decisions regarding CP for any products.

In addition, Helpson continues to explore the field of comprehensive healthcare. Comprehensive healthcare is a general concept proposed by the Chinese government according to the development of the times, social needs and changes in disease spectrum. According to the Outline of “Healthy China 2030” issued by Chinese government in October 2016, the total size of China’s health service industry is expected to reach RMB 16 trillion (approximately $2.5 trillion) by 2030. This industry focuses on people’s daily life, aging and diseases, pays attention to all kinds of risk factors and misunderstandings affecting health, calls for self-health management, and advocates the comprehensive care throughout the entire process of life. It covers all kinds of health-related information, products, and services, as well as actions taken by various organizations to meet the health needs. In response to this trend, Helpson launched Noni enzyme, a natural, Xeronine-rich antioxidant food supplement at the end of 2018. It also launched wash-free sanitizers and masks, in 2020, to address the market needs caused by COVID-19 in China. As Chinese government officially terminated its zero-case policy, now the responsibility to protect people from the impact of COVID-19 falls more to the citizens themselves, and masks and sanitizers have been popular since COVID-19. Helpson has sufficient production capacity for medical masks, surgical masks, KN95 masks, and N95 masks, which also meets the personal needs for protection against other respiratory infectious diseases. Helpson’s N95 medical protective mask has received registration certificate at the end of 2022 and has been on the market in the mainland China nationwide.

Helpson will continue to optimize its product structure and actively respond to the current health needs of human beings.

Results of Operations for the Three months ended June 30, 2025

Revenue

Revenue was $1.03 million for the three months ended June 30, 2025, which represented an increase of $0.10 million, as compared to $0.92 million for the three months ended June 30, 2024. This increase was mainly driven by fluctuating sales increases in some products during the quarter.

Set forth below are our revenues by product category in millions (USD) for the three months ended June 30, 2025 and 2024:

	Three Months Ended June 30,
Product Category	2025		2024		Net Change		% Change
CNS Cerebral & Cardio Vascular		0.42		0.37		0.05		14	%
Anti-Viral/ Infection & Respiratory		0.53		0.48		0.05		10	%
Digestive Diseases		0.06		0.04		0.02		50	%
Other		0.02		0.03		-0.01		-33	%

The most significant revenue increase in terms of dollar amount was in the “Anti-Viral/ Infection & Respiratory” category. It generated $0.53million for the three months ended June 30, 2025, compared to $0.48 million for the three months ended June 30, 2024, which represented an increase of $0.05million. This increase was mainly due to the increase in sales of the Clarithromycin due to market fluctuation.

Our “CNS Cerebral & Cardio Vascular” product category generated $0.42 million in sales revenue for the three months ended June 30, 2025, compared to $0.37 million for the same period last year, which represented an increase of $0.05 million. This increase was mainly due to the increase in sales of Alginic Sodium Diester Injection due to market fluctuation.

“Digestive” product category generated $0.06 million in sales revenue for the three months ended June 30, 2025, compared to $0.04 million for the same period last year, which represented an increase of $0.02 million. This increase was mainly due to the increase in sales of Omeprazole due to market volatility.

The “Other” product category generated $0.02 million for the three months ended June 30, 2025, compared to $0.03 million for the three months ended June 30, 2024, which represented a decrease of $0.01 million. This decrease was mainly due to the decrease in sales of the Vitamin B6 for Injection due to market fluctuation.

	Three Months Ended June 30,
Product Category	2025			2024
CNS Cerebral & Cardio Vascular		40	%		41	%
Anti-Viral/ Infection & Respiratory		52	%		52	%
Digestive Diseases		6	%		4	%
Other		2	%		3	%

For the three months ended June 30, 2025, revenue breakdown by product category experienced certain variances compared with that of the prior year. Sales in the “Anti-Viral/Infection & Respiratory” product category represented 52% of total sales in each of the three months ended June 30, 2025 and 2024, respectively. The “CNS Cerebral & Cardio Vascular” category represented 40% of total revenue for the three months ended June 30, 2025, compared to 41% for the three months ended June 30, 2024. The “Digestive Diseases” category represented 6% and 4% of total revenue for the three months ended June 30, 2025 and 2024, respectively. The “Other” category represented 2% and 3% of revenues for the three months ended June 30, 2025 and 2024, respectively.

Cost of Revenue

For the three months ended June 30, 2025, our cost of revenue was $1.11 million, or 108.5% of total revenue, which represented a decrease of $0.83 million from $1.94 million, or 209.8% of total revenue, in the same period of 2024. The decrease in cost of revenues in the three months ended June 30, 2025 was mainly due to the decrease in amortization of our PP&E.

Gross Loss and Loss Margin

Gross loss for the three months ended June 30, 2025 was $0.09 million, compared to $1.02 million for the three months ended June 30, 2024. Our gross loss margin for the three months ended June 30, 2025 was 8.5%, compared to 109.8% for the three months ended June 30, 2024. The main reasons for the improvement in the gross loss rate were: the decrease in amortization of our PP&E and the decrease in the allowance of inventory obsolescence.

Selling Expenses

Our selling expenses for the three months ended June 30, 2025 were $0.10 million, a decrease of $0.01 million compared to $0.11 million for the three months ended June 30, 2024. Selling expenses accounted for 9.9% of the total revenue for the three months ended June 30, 2025 compared to 12.0% for the three months ended June 30, 2024. Because of the adjustments in the sales practices and Chinese national CP, we reduced selling expenses to efficiently support the sales and the collection of accounts receivable, especially in the context of the increasing impact of CP, like other players in the industry, we have reduced the promotion expenses.

General and Administrative Expenses

Our general and administrative expenses for the three months ended June 30, 2025 were $0.44 million, an increase of $0.35 million compared to $0.09 million for the three months ended June 30, 2024. General and administrative expenses accounted for 43.0% and 9.9% of our total revenues for the three months ended June 30, 2025 and 2024, respectively. Reason for this increase was mainly due to the increased amortization of intangible asset.

Research and Development Expenses

Our research and development expenses were $0.02 million for the three months ended June 30, 2025 and $0.16 million for the three months ended June 30, 2024. Research and development expenses accounted for 2.0% and 17.8% of our total revenues for the three months ended June 30, 2025 and 2024, respectively. The negative research and development (R&D) expense resulted from a refund received due to the default of an outsourced project partner, which offset previously recognized costs.

Credit Losses

Our credit losses for the three months ended June 30, 2025 was $2,032, as compared to $8,476 for the same period in 2024.

In general, our normal customer credit or payment terms are 90 days. This has not changed in recent years. Such relatively long credit term is due to the peculiar environment affecting the Chinese pharmaceutical market, as deferred payments by state-owned hospitals to local drug distributors are common, and their deferred payments will indirectly delay the payments from our customers to us. Due to the timeliness requirements of the NMPA for logistics of drug sales, Helpson, like most other pharmaceutical companies in China, sells substantially all the drugs to local drug distributors, certified by GSP (Good Supply Practice), the standard of products supply, which is a standard protocol to control the quality of the products during circulation. These GSP certified distributors then sell the drugs to state-owned hospitals. The GSP certified distributors’ payments to us are usually delayed as they will pay us after they receive payment from the state-owned hospitals. Therefore, as most of our customers are GSP certified distributors, we adopt a unified policy for bad debt allowance reserves for GMP’s customers who are typically GSP certified distributors. As is typical in the Chinese pharmaceutical market, there are no written contracts between the Company and any of its GSP certified distributors requesting the distributors to pay the Company’s account receivable upon their receipt of funds from the distributors’ customers, or state-owned hospitals. Nevertheless, the Company’s customers typically process the payment of the account receivable to the Company upon their receipt of payment from their customers, i.e., the state-owned hospitals, as a matter of implied consensus or industry standard. In the event the length of collection term is deviated from any of the past pattern of any particular customer, the Company will adjust its credit term.

The amount of net accounts receivable that was past due (or the amount of accounts receivable that was more than 180 days old) was $0.08 million and $0.06 million as of June 30, 2025 and December 31, 2024, respectively.

The following table illustrates our trade accounts receivable aging distribution in terms of the percentage of the total accounts receivable, respective gross accounts receivables as well as the allocated allowance for credit losses as of June 30, 2025 and 2024:

	June 30,			December 31,
	2025			2024
1 - 180 Days		1.36	%		1.24	%
180 - 365 Days		0.63	%		0.48	%
365 - 720 Days		0.01	%		0.01	%
> 720 Days		98.00	%		98.27	%
Total		100.00	%		100.00	%

	Gross Trade Accounts Receivable Amount				Allocated Allowance for Doubtful Accounts
	30-Jun-25		31-Dec-24		30-Jun-25		31-Dec-24
1-180 Days		189,654		176,431		0		0
180-365 Days		87,286		68,322		8,729		6,832
365-720 Days		1,935		718		1,355		503
Over 720 Days		13,633,923		13,930,801		13,633,923		13,930,801
Total		13,912,799		14,176,273		13,644,006		13,938,136

Our allowance for credit losses estimate practice using the current expected credit loss method considers accounts receivable balances aged within 180 days current, except for any individual uncollectible account assessed by management. We account for the following respective percentage as credit loss allowance based on age of the accounts receivables: 10% of accounts receivable that are between 180 days and 365 days old, 70% of accounts receivable that are between 365 days and 720 days old, and 100% of accounts receivable that are greater than 720 days old.

Our allowance for credit losses as a percentage of accounts receivable of trade accounts receivable was 98.1% and 98.3% as of June 30, 2025 and December 31, 2024, respectively.

We conduct analysis and review on accounts receivables for customers on a specific, per-customer basis in the fourth fiscal quarter of each fiscal year. For customers (i) whose business license has been cancelled or expired; (ii) whose key business certificates such as GSP (Good Supply Practice) license have been invalid or revoked; (iii) who have no ability to continue operations, or (iv) who are encountering other issues that lead to accounts receivable unrecoverable, the receivable will be written-off as per the resolution of our Board of Directors.

We recognize credit losses per actual write-offs as well as changes of allowance for credit losses. To the extent that our current allowance for credit losses is higher than that of the previous period, we recognize a bad debt expense for the difference during the current period, and when the current allowance is lower than that of the previous period, we recognize a credit gains for the difference. The allowance for credit losses balances were $13.6 million as of June 30, 2025 and $13.9 million as of December 31, 2024, respectively. The changes in the allowances for credit losses of trade accounts receivable during the six months ended June 30, 2025 and 2024 were as follows:

	For the Six Months Ended June 30,
	2025		2024
Balance, Beginning of Period	$	13,587,182	$	13,786,074
Credit Losses		709		6,410
Foreign currency translation adjustment		56,115		(86,407	)
Balance, End of Period	$	13,644,006	$	13,706,077

Our credit losses for the six months ended June 30, 2025 was $709, as compared to$6,410 in the same period in 2024.

Loss from Operations

Our operating loss for the three months ended June 30, 2025 was $0.65 million, compared to $1.39 million in the same period in 2024.

Research and Development Subsidy

Our research and development subsidy for the three months ended June 30, 2025 was $0.02 million, it was resulted from a refund received due to the default of an outsourced project partner. There was no research and development subsidy in the same period last year.

Net Interest Expense

Net interest expense was $0.03 million for the three months ended June 30, 2025 and $0.05 million for the three months ended June 30, 2024.

Net Loss

Net loss for the three months ended June 30, 2025 was $0.53 million, compared to net loss of $1.44 million for the three months ended June 30, 2024. The improvement in net loss was mainly a result of the decline in cost.

Loss per basic and diluted common share was $0.16 for the three months ended June 30, 2025 and $0.89 for the three months ended June 30, 2024, respectively.

The number of basic and diluted weighted-average outstanding shares used to calculate loss per share was 3,261,911 for the three months ended June 30, 2025, as compared to 1,612,426 for the same period in 2024.

The significant change in weighted-average outstanding shares and per share figures reflects the impact of our 1-for-10 reverse stock split that became effective on April 15, 2025. While this split occurred after the quarter end, in accordance with SEC reporting requirements and U.S. GAAP, we have retrospectively adjusted all share and per share information for all periods presented. The reverse stock split reduced the number of outstanding shares by combining every 10 shares into 1 share, which has the mathematical effect of increasing the loss per share figures proportionately when comparing current results to prior periods. This stock split follows our previous 1-for-5 reverse stock split implemented on March 6, 2024.

Results of operations for the six months ended June 30, 2025

Revenue

Revenue decreased by 5.8% to $2.16 million for the six months ended June 30, 2025, as compared to $2.29 million for the six months ended June 30, 2024.

Set forth below are our revenues by product category in millions (USD) for the six months ended June 30, 2025 and 2024, respectively:

	Six Months Ended June 30,
Product Category	2025		2024		Net Change		% Change
CNS Cerebral & Cardio Vascular		0.75		0.70		0.05		7	%
Anti-Viral/ Infection & Respiratory		1.25		1.40		-0.15		-11	%
Digestive Diseases		0.11		0.08		0.03		38	%
Other		0.04		0.11		-0.07		-64	%

The most significant revenue increase in terms of dollar amount was our “CNS Cerebral & Cardio Vascular” product category, which generated $0.75 million in sales revenue in the six months ended June 30, 2025 compared to $0.70 million in the same period a year ago, represented an increase of $0.05 million that was mainly caused by the increase in sales of Alginic Sodium Diester Injection due to market volatility.

Sales of our “Digestive Diseases” was $0.11 million in sales revenue in the six months ended June 30, 2025, compared to $0.08 million in the same period a year ago, which represented an increase of $0.03 million. This increase was mainly due to sales increase in Omeprazole due to market volatility.

Sales of “Anti-Viral/ Infection & Respiratory” product category generated $1.25 million in sales revenue in the six months ended June 30, 2025, compared to $1.40 million in the same period a year ago, which represented a decrease of $0.15 million. This change was mainly caused by the decrease in sales of Cefaclor Dispersible Tablets due to market volatility.

Sales of our “Other” product category generated $0.04 million in the six months ended June 30, 2025, and $0.11 million in the six months ended June 30, 2024. This change was mainly due to market volatility.

	Six Months Ended June 30,
Product Category	2025			2024
CNS Cerebral & Cardio Vascular		35	%		30	%
Anti-Viral/ Infection & Respiratory		58	%		61	%
Digestive Diseases		5	%		4	%
Other		2	%		5	%

For the six months ended June 30, 2025, revenue breakdown by product category remained similar to that of the same period in 2023. The “Anti-Viral/Infection & Respiratory” products category represented 58% and 61% of total revenues in the six months ended June 30, 2025 and 2024. The “CNS Cerebral & Cardio Vascular” category represented 35% and 30% of total revenue in the six months ended June 30, 2025 and 2024, respectively. The “Digestive Diseases” category represented 5% and 4% of total revenue in the six months ended June 30, 2025 and 2024, respectively. And the “Others” category represented 2% and 5% of revenues in the six months ended June 30, 2025 and 2024, respectively.

Cost of Revenue

For the six months ended June 30, 2025, our cost of revenue was $2.39 million, or 110.3% of total revenue, comparing to $3.60 million, or 156.9% of total revenue, in the same period in 2024. The decrease in the cost to revenue in this period was mainly due to the decrease in amortization of our PP&E and the decrease in the allowance of inventory obsolescence.

Gross Loss and Loss Margin

Gross loss for the six months ended June 30, 2025 was $0.22 million, compared to $1.31 million in the same period in 2024. Our gross loss margin in the six months ended June 30, 2025 was 10.3% compared to 56.9% in the same period in 2024. The improvement of gross margin in this period was mainly due to the decrease in amortization of our PP&E and the decrease in the allowance of inventory obsolescence.

Selling Expenses

Our selling expenses for the six months ended June 30, 2025 and 2024 were $0.19 million and $0.22 million, respectively. Selling expenses accounted for 8.7% of the total revenue in the six months ended June 30, 2025 compared to 9.6% in the same period in 2024.

General and Administrative Expenses

Our general and administrative expenses for the six months ended June 30, 2025 were $0.95 million, as compared to $0.58 million in the same period in 2024. Our general and administrative expenses accounted for 43.8% and 25.3% of our total revenues in the six months ended June 30, 2025 and 2024, respectively.

Research and Development Expenses

Our research and development expenses for the six months ended June 30, 2025 and 2024 were $0.05 million and $0.20 million, respectively.

Loss from Operations

Our operating loss for the six months ended June 30, 2025 was $1.41 million, compared to $2.31 million in the same period in 2024. The decrease in loss from operation is mainly due to the decrease in amortization of our PP&E and the decrease in the allowance of inventory obsolescence.

Net Interest Expense

Net interest expense for the six months ended June 30, 2025 was $0.05 million, compared to $0.09 million for the same period in 2024.

Net Loss

Net loss for the six months ended June 30, 2025 was $1.31 million, as compared to net loss of $2.39 million for the six months ended June 30, 2024. The decrease of net loss was mainly a result of the decrease in amortization of our PP&E and the decrease in the allowance of inventory obsolescence in this period.

For the six months ended June 30, 2025, loss per basic and diluted common share was $0.40, compared to loss per basic and diluted common share of $1.63 for the six months ended June 30, 2024.

The number of basic and diluted weighted-average outstanding shares used to calculate loss per share was 3,261,911 for the six months ended June 30, 2025, and 1,472,743 for the six months ended June 30, 2024.

Liquidity and Capital Resources

Our principal source of liquidity is cash generated from operations and bank lines of credit. Currently the Company has not witnessed or expected to encounter any difficulties to refinance those lines of credit this year. As of June 30, 2025, the aggregated advance from our CEO was $1.40 million for use in operations. Our cash and cash equivalents were $0.63 million, representing 4.5% of our total assets, as of June 30, 2025, as compared to $0.63 million, representing 4.2% of our total assets as of December 31, 2024. All of the $0.63 million of cash and cash equivalents as of June 30, 2025 are considered to be reinvested indefinitely in the Company’s Chinese subsidiary, Helpson and are not expected to be available for payment of dividends or for other payments to its parent company or to its shareholders.

The Company obtained various lines of credit which details were described under Note 8 to its unaudited consolidated financial statements contained in this report which is incorporated by reference herein.

China Pharma issued a convertible note to an institutional accredited investor as disclosed in Note 9 to the audited consolidated financial statements contained in this report which is incorporated by reference herein.

Although the Company obtained additional lines of credit for the three months ended June 30, 2025, there can be no assurance that the Company will be able to achieve its future strategic goals, including the launch of new products. This raises substantial doubt about the Company’s ability to continue as a going concern. Although our Chairperson and Chief Executive Officer had advanced funds for working capital for the three months ended June 30, 2025, there can be no assurances that this will continue in the future. We may seek additional debt or equity financing as necessary when we believe the market conditions are the most advantageous to us and/or require us to reduce certain discretionary spending, which could have a material adverse effect on our ability to achieve our business objectives. There can be no assurance that any additional financing will be available on acceptable terms, if at all.

Operating Activities

Net cash used in operating activities was $0.23 million in the six months ended June 30, 2025, compared to $0.66 million of net cash generated in the same period in 2024.

As of June 30, 2025, our net trade accounts receivable was $0.27 million, an increase of $0.04 million from $0.23 million as of December 31, 2024.

As of June 30, 2025, total inventory was $1.68 million, compared to $2.27 million as of December 31, 2024.

Investing Activities

During the six months ended June 30, 2025, net cash used in investing activities was $0.09 million. This was mainly due to the investment in purchasing of equipment, and the development of a medicine formula. And there was $0.03 million used in investing activities for the six months ended June 30, 2024.

Financing Activities

Cash flow used by financing activities was $0.09 million in the six months ended June 30, 2025; compared to $0.01 million provided in the same period in 2024.

According to relevant PRC laws, companies registered in the PRC, including our PRC subsidiary, Helpson, are required to allocate at least ten percent (10%) of their after-tax net income, as determined under the accounting standards and regulations in the PRC, to statutory surplus reserve accounts until the reserve account balances reach fifty percent (50%) of the companies’ registered capital prior to their remittance of funds out of the PRC. Allocations to these reserves and funds can only be used for specific purposes and are not transferrable to the parent company in the form of loans, advances or cash dividends. As of June 30, 2025 and December 31, 2024, Helpson’s net assets totaled ($7,187,000) and ($6,197,000), respectively. Due to the restriction on dividend distribution to overseas shareholders, the amount of Helpson’s net assets that was designated for general and statutory capital reserves, and thus could not be transferred to our parent company as cash dividends, was 50% of Helpson’s registered capital, which was both $8,145,000 as of June 30, 2025 and December 31, 2024, respectively. The amount that Helpson must set aside for the statutory surplus fund accounts exceeds its total net assets as of June 30, 2025 and December 31, 2024. There were no allocations to the statutory surplus reserve accounts during the six months ended June 30, 2025.

The Chinese government also imposes controls on the conversion of RMB into foreign currencies and the remittance of currencies out of China. Our businesses and assets are primarily denominated in RMB. All foreign exchange transactions take place either through the People’s Bank of China or other banks authorized to buy and sell foreign currencies at the exchange rates quoted by the People’s Bank of China. Approval of foreign currency payments by the People’s Bank of China or other regulatory institutions requires the submission of a payment application form together with certain invoices and executed contracts. The currency exchange control procedures imposed by Chinese government authorities may restrict Helpson, our Chinese subsidiary, from transferring its net assets to our parent company through loans, advances or cash dividends.

Off-Balance Sheet Arrangements

As of June 30, 2025, we did not have any off-balance sheet arrangements.

Critical Accounting Policies

Management’s discussion and analysis of our financial condition and results of operations are based upon our consolidated financial statements, which have been prepared in accordance with United States generally accepted accounting principles. Our financial statements reflect the selection and application of accounting policies which require management to make significant estimates and judgments. The discussion of our critical accounting policies contained in Note 1 to our consolidated financial statements, “Organization and Significant Accounting Policies”, included in the Company’s annual report on Form 10-Q for the six months ended June 30, 2025, which is incorporated herein by reference.

Item 3. Quantitative and Qualitative Disclosures about Market Risk

As a “smaller reporting company” as defined by Item 10 of Regulation S-K, we are not required to provide information required by this item.

Item 4. Controls and Procedures

Evaluation of Disclosure Controls and Procedures

Our Chief Executive Officer and interim Chief Financial Officer, evaluated the effectiveness of our “disclosure controls and procedures” (as defined in the Securities Exchange Act of 1934 (the “Exchange Act”) Rules 13a-15(e) or 15d-15(e)) as of the end of the period covered by this quarterly report. Disclosure controls and procedures are controls and other procedures that are designed to ensure that information required to be disclosed in our reports filed or submitted under the Exchange Act (a) is recorded, processed, summarized and reported within the time periods specified in the Securities and Exchange Commission’s rules and forms and (b) is accumulated and communicated to management, including our Chief Executive Officer and interim Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. Our management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives and management necessarily applies its judgment in evaluating the cost-benefit relationship of possible controls and procedures.

Our disclosure controls and procedures are designed to provide reasonable assurance of achieving their objectives as described above. Based on this evaluation, our Chief Executive Officer and interim Chief Financial Officer concluded that our disclosure controls and procedures were not effective as of June 30, 2025 to satisfy the objectives for which they are intended. This was due to the material weakness in our internal control over financial reporting, with respect to our lack of accounting financial reporting personnel who were knowledgeable in U.S. GAAP, as disclosed in our annual report on Form 10-K for the fiscal year ended December 31, 2024, filed with the SEC on March 31, 2025. Notwithstanding the aforementioned material weakness, management has concluded that our condensed consolidated financial statements included in this report are fairly stated in all material respects in accordance with U.S. GAAP for each period presented herein.

Changes in Internal Controls over Financial Reporting

There were no changes in our internal control over financial reporting identified in connection with the evaluation required by paragraph (d) of Exchange Act Rules 13a-15 or 15d-15 that occurred during our last fiscal quarter that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

PART II OTHER INFORMATION

Item 6. Exhibits

The exhibits required by this item are set forth in the Exhibit Index attached hereto.

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

	CHINA PHARMA HOLDINGS, INC.

Date: August 14, 2025	By:	/s/ Zhilin Li
		Name:	Zhilin Li
		Title:	President and Chief Executive Officer
			(principal executive officer)

Date: August 14, 2025	By:	/s/ Zhilin Li
		Name:	Zhilin Li
		Title:	Interim Chief Financial Officer
			(principal financial officer and principal accounting officer)

EXHIBIT INDEX

No.		Description

3.1		The Third Amended and Restated Articles of Incorporation of the Company (incorporated by reference to Exhibit 3.1 to our Quarterly Report on Form 10-Q filed on May 14, 2025).

31.1 -		Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.2 -		Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

32.1 -		Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

101.INS -		XBRL Instance Document

101.SCH -		XBRL Taxonomy Extension Schema Document

101.CAL -		XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF -		XBRL Taxonomy Extension Definition Linkbase Document

101.LAB -		XBRL Taxonomy Extension Label Linkbase Document

101.PRE -		XBRL Taxonomy Extension Presentation Linkbase Document

104 -		Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)

SEC Form 10-Q filed by China Pharma Holdings Inc.