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 ...
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 ...
Pepcid products are commonly used to prevent and treat heartburn caused by acid indigestion and upset stomach. The main active ingredient in Pepcid is famotidine, which belongs to a class of medicines ...
(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 ...
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 ...
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 ...
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, ...
In the table of the release dated Nov 6, 2025, First Ship Date for Batch Number 6133388 should be 04/15/2025.
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, ...
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