FDAJanuary 7, 2020drug

Ranitidine Capsules 300 mg, 30 count bottles. Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623, NDC 62559-691-30.

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

appco pharmaappco

Recall history

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

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