FDADecember 26, 2019drug

Ranitidine 150 mg tablets, 130 count bottles, NDC 37808-196-04.

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

The hazard

CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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