FDAApril 6, 2022drug

Losartan Potassium 50 mg Tablet, a) 30-count blister card (NDC# 70518-3282-1), b) 60-count blister card (NDC: 70518-3282-0), Rx Only, MFG by: Lupin Pharma, Baltimore, MD 21202.

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

The hazard

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

What to do

FDA enforcement status: Terminated

Brands named

remedyrepack

Recall history

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

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