But we still have more questions than answers
Also included are 2015 through 2019 Golf Sportwagens, and
Famotidine is used to treat stomach ulcers (gastric and duodenal), erosive esophagitis (heartburn or acid indigestion), and gastroesophageal reflux disease (GERD)
(JJMCP) is initiating a voluntary recall of one lot of PEPCID® COMPLETE®, lot number BEF062, and one lot of ORIGINAL STRENGTH PEPCID® AC®, lot number BFF010, from the wholesaler and retailer level
Studies have not assessed the safety of famotidine in uncomplicated active duodenal ulcer for periods of more than eight weeks
The new Zantac medication, Zantac 360, contains the active ingredient famotidine instead of ranitidine
We enrolled patients who were using ranitidine or famotidine for more than
On March 10, 2021, AUROBINDO PHARMA recalled FAMOTIDINE 40MG due to the possibility of a tablet mix-up
and Perrigo has joined the recall after testing Teva Pharmaceuticals has initiated a voluntary recall in the United States, to the patient level, 4/2019: Amlodipine and Valsartan Tablets 5 mg/160 mg: 30 Count: 0093-7690-56: 23X023: Manufacturers and big pharmacies are recalling Zantac after the FDA announced it was investigating low-levels of cancer-causing chemicals in the popular heartburn drug
279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India, NDC 65862-860-99 The
30, 2019
is recalling item #922982 Kirkland Signature Acid Reducer 150 mg because it may contain the impurity N-nitrosodimethylamine (NDMA) above acceptable levels
When constituted as directed, famotidine for oral suspension is a smooth, mobile, white to off-white, homogeneous suspension with a cherry-banana-mint flavor, 4
Drug interactions with famotidine are uncommon
The recall included all prescription and over-the-counter (OTC) Medications such as famotidine (Pepcid®), cimetidine (Tagamet®), esomeprazole (Nexium®), lansoprazole (Prevacid®), and omeprazole (Prilosec®) are available both by prescription and OTC to help manage these conditions
The FDA has also urged a voluntary recall of nizatidine (Axid), due to the detection of NDMA in some batches