Ranitidine (Zinetac ) is an antacid, antireflux agent and antiulcerant, prescribed for peptic ulcer. It decreases the amount of acid made in the stomach. The information provided on this page is ...

The study aimed to assess the efficacy, safety, and tolerability of Ranitidine HCl 150/300 mg tablets (Rantac® 150/Rantac® 300/Rantac® OD 300 of J. B. Chemicals and Pharmaceuticals Ltd.) among Indian ...

Pharmascience Inc. is recalling 30 lots of over-the-counter ranitidine drugs (150 mg tablets), packaged in blister packs, after tests found NDMA, a nitrosamine impurity, above the acceptable level in ...

of ranitidine HCl capsules in 150 mg and 300 mg strengths (15). Denton Pharma also recalled all unexpired lots of ranitidine tablets, 150 mg and 300mg, in response to the manufacturer’s recall of all ...

Pharmascience Inc. is recalling 13 lots of prescription and over-the-counter ranitidine drugs (150 mg tablets) after tests found NDMA, a nitrosamine impurity, at below but close to the accepted level.

UPDATE: February 5, 2021 – Pharmascience Inc. recalls certain lots of prescription and over-the-counter ranitidine as a precaution Pharmascience Inc. is recalling 13 lots of prescription and ...

Pharmascience Inc. is recalling 23 additional lots of its over-the-counter ranitidine drugs (75 mg tablets) after tests found NDMA, a nitrosamine impurity, above accepted levels. Please refer to ...

Pharmascience Inc. recalled one lot of prescription PMS-Ranitidine (150 mg strength tablet) as a precaution after tests found N-nitrosodimethylamine (NDMA), a nitrosamine impurity, at close to the ...

2020 /CNW/ - Pharmascience Inc. is recalling one lot of prescription PMS-Ranitidine (150 mg strength tablet) as a precaution after tests found NDMA, a nitrosamine impurity, at close to the accepted ...

The company has made a decision to discontinue the manufacture and supply of Zinetac tablets (150 mg and 300 mg products ... of cancer-causing N-Nitrosodimethylamine (NDMA) in Zinetac (ranitidine) ...

American Health Packaging has voluntarily recalled eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters to the consumer level due to the potential N ...