FDAJune 14, 2019drug

Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90

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: Terminated

Brands named

golden state medical supplygoldengolden state

Recall history

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

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Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90 — Recall Details · AllClear