FDAJune 6, 2019drug

LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles, NDC 00591-3746-00

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

The hazard

CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.

What to do

FDA enforcement status: Ongoing

Brands named

teva pharmaceuticalsteva

UPCs

00591374600

Recall history

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

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