Famotidine (Febcid (20 mg)) is a histamine (H2-receptor antagonist), prescribed for ulcer. It works by decreasing the amount of stomach acid. The information provided on this page is intended to serve ...
Johnson & Johnson-Merck Consumer Pharmaceuticals Company has received the approval from the U.S. Food and Drug Administration (FDA) for Maximum Strength Pepcid AC (famotidine 20 mg) for ...
Famotidine Injection is indicated in some hospitalized patients with pathological hypersecretory conditions or intractable ulcers, or as an alternative to the oral dosage forms for short term use in ...
OKLAHOMA CITY, OK, January 10, 2007 – In a new study, researchers have directly compared the early therapeutic response of drugs from widely-used classes of heartburn medications, omeprazole magnesium ...
(RTTNews) - Dr. Reddy's Laboratories Ltd. (DRREDDY, RDY) announced Tuesday the re-launch of over-the-counter or OTC Famotidine Tablets USP, 10 mg and 20 mg, in the U.S. market. OTC Famotidine Tablets ...
HYDERABAD, India & PRINCETON, N.J.--(BUSINESS WIRE)-- Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, along with its subsidiaries together referred to as “Dr. Reddy’s”) today ...
FOR IMMEDIATE RELEASE – Nov. 6,2025 – LAKE ZURICH, Ill.— Fresenius Kabi, part of the global healthcare company Fresenius, and a leading provider of essential medicines and medical technologies is ...
Fresenius Kabi, part of the global healthcare company Fresenius, and a leading provider of essential medicines and medical technologies is voluntarily recalling three lots (numbers 6133156, 6133194, ...
Three lots (numbers 6133156, 6133194, 6133388) of Famotidine Injection are being recalled in the U.S. by Fresenius Kabi. Three lots (numbers 6133156, 6133194, 6133388) of Famotidine Injection are ...
In the table of the release dated Nov 6, 2025, First Ship Date for Batch Number 6133388 should be 04/15/2025. FRESENIUS KABI ISSUES VOLUNTARY NATIONWIDE RECALL OF THREE LOTS OF FAMOTIDINE INJECTION, ...