FDAJuly 18, 2018drug

AvKARE Valsartan and Hydrochlorothiazide 80 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-884-90

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

The hazard

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

What to do

FDA enforcement status: Terminated

Brands named

avkare

Recall history

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

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