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FDAOctober 1, 2019drug

Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.) 220 count bottles (NDC 49035-404-65) (Walmart) OTC

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

The hazard

CGMP Deviations: Presence of NDMA impurity detected in product.

What to do

FDA enforcement status: Completed

Brands named

dr reddy s laboratories

Recall history

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

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