Glenmark Pharmaceuticals Inc., USA Recalls

2 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.

Nov 21, 2025

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Cross Contamination

Health & Personal Care

HIGH

FDA DRUG

Glenmark Carvedilol 25 mg Recall Expands Over NNCI Impurity Above FDA Limit in 14,976 Bottles

Glenmark Pharmaceuticals recalls 14,976 bottles of Carvedilol 25 mg distributed nationwide in the United States after FDA-identified NNCI impurity exceeds limits. The impurity prompted CGMP deviation findings. Consumers should stop taking the drug and contact Glenmark or a healthcare provider for guidance.

Aug 6, 2025

CARVEDILOL

CGMP Deviations:

Brand Statistics

Total Recalls

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Glenmark Pharmaceuticals Inc., USA Recalls

Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination

Glenmark Carvedilol 25 mg Recall Expands Over NNCI Impurity Above FDA Limit in 14,976 Bottles

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