Jul 30, 2024   SOURCE: PR NewsWire

CUMBERLAND PHARMACEUTICALS TO ANNOUNCE SECOND QUARTER 2024 FINANCIAL RESULTS

NASHVILLE, Tenn., July 30, 2024 /PRNewswire/ -- Cumberland Pharmaceuticals Inc. (Nasdaq: CPIX), a specialty pharmaceutical company, announced today that it will release its second quarter 2024 financial results and provide a company update after the market closes on Tuesday, Aug. 6, 2024.

A conference call will be held on Aug. 6 at 4:30 p.m. Eastern Time to discuss the results. To participate in the call, please register at https://register.vevent.com/register/BIfa6a94515e5548c28e9d77d03c95a13e.

Once registered, participants can dial in from their phone using a dial-in and PIN number that will be provided to them. Alternatively, they can choose a "Call Me" option to have the system automatically call them at the start of the conference.

A replay of the call will be available for one year and can be accessed via Cumberland's website or by visiting https://edge.media-server.com/mmc/p/h9bx4zn8.

Cumberland Pharmaceuticals is a specialty pharmaceutical company focused on providing unique products that improve patient care. The company develops, acquires, and commercializes products for the hospital acute care, gastroenterology and oncology market segments.

The company's portfolio of FDA-approved brands includes:

    --  Acetadote(®) (acetylcysteine) injection, for the treatment of
        acetaminophen poisoning;
    --  Caldolor(®) (ibuprofen) injection, for the treatment of pain and fever;
    --  Kristalose(®) (lactulose) for oral solution, a prescription laxative,
        for the treatment of constipation;
    --  Omeclamox(®)-Pak, (omeprazole, clarithromycin, amoxicillin) for the
        treatment of Helicobacter pylori (H. pylori) infection and related
        duodenal ulcer disease;
    --  Sancuso(®) (granisetron) transdermal system, for the prevention of
        nausea and vomiting in patients receiving certain types of chemotherapy
        treatment;
    --  Vaprisol(®) (conivaptan) injection, to raise serum sodium levels in
        hospitalized patients with euvolemic and hypervolemic hyponatremia; and
    --  Vibativ(®) (telavancin) injection, for the treatment of certain serious
        bacterial infections including hospital-acquired and
        ventilator-associated bacterial pneumonia, as well as complicated skin
        and skin structure infections.

The company also has a series of Phase II clinical programs underway evaluating its ifetroban product candidate in patients with cardiomyopathy associated with Duchenne Muscular Dystrophy and Systemic Sclerosis. Additionally, Cumberland recently received FDA clearance to proceed directly to a Phase II study for patients with Idiopathic Pulmonary Fibrosis, the most common form of progressive fibrosing interstitial lung disease.

For more information on Cumberland's approved products, including full prescribing information, please visit links to the individual product websites, which can be found on the company's website at www.cumberlandpharma.com.

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SOURCE Cumberland Pharmaceuticals