AVKARE Inc.: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Dose
Recall reason: CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.. Recalled by AVKARE Inc.. Distribution: Nationwide. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot: 20121 Exp. 6/30/2019. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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