Glenmark Pharmaceuticals Inc., USA Recalls

3 recalls found for Glenmark Pharmaceuticals Inc., USA. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination

Glenmark Pharmaceuticals recalled over 11,000 bottles of Bisoprolol Fumarate and Hydrochlorothiazide Tablets on November 21, 2025. Testing revealed traces of ezetimibe, posing a health risk. Consumers should stop using the product immediately and contact their healthcare provider.

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
Cross Contamination
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Carvedilol Tablets Due to Impurity Hazard

Glenmark Pharmaceuticals recalled 14,976 bottles of Carvedilol Tablets on August 6, 2025. The recall follows findings of N-Nitroso Carvedilol Impurity-1 above FDA limits. Consumers should stop using the product immediately and contact their healthcare provider.

CARVEDILOL
CGMP Deviations:
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Brand Statistics

Total Recalls
3
Pages
1

Related Brands

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDECARVEDILOL