Teva Pharmaceuticals USA: LOSARTAN POTASSIUM TABLETS, USP 100 mg, Bulk
Recall reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.. Recalled by Teva Pharmaceuticals USA. Distribution: Bulk product was distributed to one re-packager in California.. Classification (Class II — potential health risk). Affected lots/NDC/dates: 1178533A, 1178534A, 1178535A, 1178536A, 1178537A, 1178538A, 1178539A, 1178540A, 1178541A, 1178542A, 1178543A,. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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