NASHVILLE, Tenn., Oct. 31, 2017 /PRNewswire/ -- Cumberland Pharmaceuticals Inc. (NASDAQ: CPIX) announced today that it will release third quarter 2017 financial results after the market closes on Tuesday, November 7, 2017. A conference call and live Internet webcast will be held on Tuesday, November 7, 2017, at 4:30 p.m. Eastern Time to discuss the results.

To participate in the call, please dial 877-303-1298 (for U.S. callers) or 253-237-1032 (for international callers). A rebroadcast of the teleconference will be available for one week and can be accessed by dialing 855-859-2056 (for U.S. callers) or 404-537-3406 (for international callers). The Conference ID for the rebroadcast is 5299837. The live webcast and rebroadcast can be accessed via Cumberland's website at http://investor.shareholder.com/cpix/events.cfm.

Cumberland Pharmaceuticals Inc. is a specialty pharmaceutical company focused on the delivery of high-quality prescription brands to improve patient care. The Company develops, acquires, and commercializes brands 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 chronic and acute constipation;
    --  Omeclamox(®)-Pak, (omeprazole, clarithromycin, amoxicillin) for the
        treatment of Helicobacter pylori (H. pylori) infection and related
        duodenal ulcer disease;
    --  Vaprisol(®) (conivaptan) Injection, to raise serum sodium levels in
        hospitalized patients with euvolemic and hypervolemic hyponatremia;
    --  Ethyol(®) (amifostine) Injection, for the reduction of xerostomia (dry
        mouth) in patients undergoing post-operative radiation treatment for
        head and neck cancer and the renal toxicity associated with the
        administration of cisplatin in patients with advanced ovarian cancer;
    --  Totect(®) (dexrazoxane hydrochloride) Injection, for emergency oncology
        intervention, to treat the toxic effects of anthracycline chemotherapy
        in case of extravasation (drug leakage from the bloodstream into the
        tissues).

Cumberland's pipeline of product candidates includes:


    --  Hepatoren(®) (ifetroban) Injection, a Phase II candidate for the
        treatment of critically ill patients suffering from liver and kidney
        failure associated with hepatorenal syndrome ("HRS");
    --  Boxaban(®) (ifetroban) oral capsules, a Phase II candidate for the
        treatment of asthma patients with aspirin-exacerbated respiratory
        disease ("AERD");
    --  Vasculan(TM) (ifetroban) oral capsules, a Phase II candidate for the
        treatment of patients with the systemic sclerosis (SSc) form of
        autoimmune disease;
    --  Portaban(TM) (ifetroban) oral formulation, a Phase II candidate for the
        treatment of patients with portal hypertension associated with liver
        disease;
    --  Methotrexate (methotrexate) Injection, an approval submission candidate
        for the treatment of active rheumatoid, juvenile idiopathic and severe
        psoriatic arthritis, as well as severe disabling psoriasis.

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

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SOURCE Cumberland Pharmaceuticals Inc.