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FDAOctober 23, 2019drug

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 60 tablets per bottle. [NDC: Brand] NDC Health Mart: 62011-0283-2; NDC Major: 0904-6715-52; NDC Meijer: 41250-252-72; NDC Sunmark: 49348-136-12;

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

What to do

FDA enforcement status: Terminated

Brands named

perrigo company plcperrigoperrigo company

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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