Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10

Recall Number: D-1464-2019

Firm: Golden State Medical Supply Inc.

Classification: Class II

Status: Terminated

Report Date: 20190717

Initiation Date: 20190614

Termination Date: 20200219

Reason for Recall

CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.

Product Description

Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10

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