FDAMarch 5, 2019drug

Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-513-15

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

The hazard

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified

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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Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-513-15 — Recall Details · AllClear