Glenmark Pharmaceuticals Inc. Recalls

4 recalls found for Glenmark Pharmaceuticals Inc.. Check if any of your products are affected.

HIGHFDA DRUG

Glenmark Pharmaceuticals Recalls Ondansetron Tablets Over Packaging Issues

Glenmark Pharmaceuticals recalled nearly 97,000 packs of Ondansetron Orally Disintegrating Tablets on December 30, 2025. Defective blister packs may not fully seal, leading to tablets falling out. Consumers should stop using the product immediately and contact healthcare providers.

ONDANSETRON
Defective container:
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HIGHFDA DRUG

Glenmark Pharmaceuticals Recalls Viorele Tablets Over Impurity Issues

Glenmark Pharmaceuticals recalled 26,928 packs of Viorele oral contraceptives on September 3, 2025. The recall follows the discovery of impurity issues in the product. Consumers should stop using the affected tablets immediately and contact healthcare providers for guidance.

Viorele
Failed Impurities/Degradation
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HIGHFDA DRUG

Glenmark Pharmaceuticals Recalls Theophylline Tablets Over Dissolution Issues

Glenmark Pharmaceuticals Inc. recalled 22,656 bottles of Theophylline extended-release tablets on August 8, 2025. The recall follows reports of failed dissolution specifications that could impact medication efficacy. Consumers should stop using the product and consult healthcare providers immediately.

Glenmark Pharmaceuticals Inc.
Failed Dissolution
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HIGHFDA DRUG

Glenmark Pharmaceuticals Recalls Carvedilol Tablets Over Contaminant

Glenmark Pharmaceuticals recalled 6,432 bottles of Carvedilol Tablets on August 7, 2025. The recall stems from CGMP deviations due to the presence of a nitrosamine impurity above acceptable levels. Consumers should stop using the product immediately and contact healthcare providers for guidance.

Glenmark Pharmaceuticals Inc.
CGMP Deviations:
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Brand Statistics

Total Recalls
4
Pages
1