Ondansetron Odt Tablets, Usp 4mg, 1x10 Unit Dose Tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged By Preferred Pharmaceuticals Ndc 68788-8666-01
Ondansetron ODT 4mg tablets manufactured by Glenmark and repackaged by Preferred Pharmaceuticals are being recalled because the blister pack seals are defective and tablets are falling out. The affected product has NDC number 68788-8666-01 and was distributed nationwide in the USA. This is a Class I recall, the most serious classification.
- Recalling firm
- Preferred Pharmaceuticals, Inc.
- Product
- Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01
- Reason
- 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.
- Classification
- Class I
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2025-11-17
- Status
- Ongoing
- Areas affected
- IN
- Distribution
- Natinowide in the USA
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/85162bc7-7bcf-4416-ba7f-3959db720532