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FDAFDA · Food and drugs·Recall number D-0246-2026

Ondansetron Orally Disintegrating Tablets, USP, 4mg, 30 Tablets (3 blistercards each containing 10 tablets), Rx only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-157-13

Published January 7, 2026 · Recall initiated: December 30, 2025

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
ONDANSETRON
Manufacturer
Glenmark Pharmaceuticals Inc., USA
Distributor
Nationwide within the United States
UPC
0368462157138
Lot
Lot #: 19251311, Exp Date April 2027
Risk classification
Class II
Area (FDA)
drug
Country
United States

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