FDAMarch 14, 2019drug

Losartan 50mg Tablet, 30 count each blister card.

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

The hazard

CGMP Deviations; Detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) - N-Methylnitrosobutyric acid (NMBA).

What to do

FDA enforcement status: Terminated

Brands named

remedyrepack

UPCs

70518058801

Recall history

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

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