NASHVILLE, Tenn., Feb. 27,
2024 /PRNewswire/ -- Cumberland Pharmaceuticals
Inc. (NASDAQ: CPIX), a specialty pharmaceuticals company,
announced today that it will release its annual 2023 financial
results and provide a company update after the market closes on
Tuesday, March 5, 2024.
A conference call will be held on March
5 at 4:30 p.m. Eastern Time to
discuss the results. To participate in the call, please register at
https://register.vevent.com/register/BI77538b1a0c52414b9e2772846f5498ae.
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/eubuwzon.
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 Inc.