Losartan 50mg Tablet, 30 count each blister card.

Recall Number: D-1081-2019

Firm: RemedyRepack Inc.

Classification: Class II

Status: Terminated

Report Date: 20190417

Initiation Date: 20190314

Termination Date: 20190411

Reason for Recall

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

Product Description

Losartan 50mg Tablet, 30 count each blister card.