FDA-Drug2025-12-10Class IIICHEMICAL

Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 2.5 mg/6.25 mg, packaged as (a) 30-count bottles, NDC-68462-878-30; (b) 100-count bottle, NDC-68462-878-01; (c) 500-count bottles, NDC-68462-878-05; Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, Inda. Manufactured for: Glenmark Pharmaceuticals, Inc., USA, Mahwah, NJ 07430.

UNDECLARED INGREDIENTSNationwide distributionDrugs
Hazard

Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe

Intended for
Adults
Illnesses reported
None reported
Sold states
Nationwide in the USA
Affected count
11,136 bottles
Manufactured in
619 River Dr, Elmwood Park, NJ, United States
Products
Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 2.5 mg/6.25 mg, packaged as (a) 30-count bottles, NDC-68462-878-30; (b) 100-count bottle, NDC-68462-878-01; (c) 500-count bottles, NDC-68462-878-05; Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, Inda. Manufactured for: Glenmark Pharmaceuticals, Inc., USA, Mahwah, NJ 07430.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0199-2026

More Glenmark recalls

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