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    Sunshine Biopharma Launches Two New Generic Prescription Drugs

    9/26/24 8:00:00 AM ET
    $SBFM
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $SBFM alert in real time by email

    FORT LAUDERDALE, FL / ACCESSWIRE / September 26, 2024 / Sunshine Biopharma, Inc. (NASDAQ:SBFM) (the "Company"), a pharmaceutical company offering and researching life-saving medicines in a variety of therapeutic areas including oncology and antivirals today announced that its wholly owned Canadian subsidiary, Nora Pharma Inc., has launched two new generic prescription drugs.

    The first product is Varenicline, a generic version of Champix®. Varenicline is used as a smoking cessation product and is available in formats of 0.5 mg and 1 mg tablets, as well as a convenient starter kit.

    The second is Betahistine, a generic version of Serc®, to treat patients with vertigo. Betahistine is available in formats of 8 mg, 16 mg and 24 mg scored tablets.

    "Propelled by Sunshine Biopharma's strategic support, Nora Pharma plans to continue its rapid top-line and bottom-line growth," said Mr. Malek Chamoun, president of Nora Pharma.

    "The addition of these two new products to our existing portfolio of 61 products will strengthen our presence in the Canadian $9.7 billion a year generic drug market," said Dr. Steve Slilaty, CEO of Sunshine Biopharma. "We look forward to additional launches later this year and next year."

    About Sunshine Biopharma

    Sunshine Biopharma currently has 61 generic prescription drugs on the market in Canada and 32 additional drugs scheduled to be launched in the remainder of 2024 and in 2025. Among the new drugs to be launched in 2024 is NIOPEG®, a biosimilar of NEULASTA®. Like NEULASTA®, NIOPEG® is a long-acting form of recombinant human granulocyte colony-stimulating factor (filgrastim). It is indicated to decrease the incidence of infection in patients with non-myeloid malignancies receiving anti-neoplastic therapy.

    In addition, Sunshine Biopharma is conducting a proprietary drug development program which is comprised of (i) K1.1 mRNA, an mRNA-Lipid Nanoparticle targeted for liver cancer, and (ii) PLpro protease inhibitor, a small molecule for treatment of SARS Coronavirus infections, including Long-Covid. For more information, please visit: www.sunshinebiopharma.com.

    All registered trademarks are the property of their respective owners.

    Safe Harbor Forward-Looking Statements

    This press release contains forward-looking statements which are based on current expectations, forecasts, and assumptions of Sunshine Biopharma, Inc. (the "Company") that involve risks as well as uncertainties that could cause actual outcomes and results to differ materially from those anticipated or expected. These statements appear in this release and include all statements that are not statements of historical fact regarding the intent, belief or current expectations of the Company, including statements related to the Company's drug development activities, financial performance, and future growth. These risks and uncertainties are further described in filings and reports by the Company with the U.S. Securities and Exchange Commission (SEC). Actual results and the timing of certain events could differ materially from those projected in or contemplated by the forward-looking statements due to a number of factors detailed from time to time in the Company's filings with the SEC. Reference is hereby made to cautionary statements and risk factors set forth in the Company's most recent SEC filings.

    For Additional Information Contact:

    Camille Sebaaly, CFO
    Direct Line: 514-814-0464
    [email protected]

    SOURCE: Sunshine Biopharma, Inc.



    View the original press release on accesswire.com

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