NDC 68462-105 – Ondansetron
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-105
Product details
- Brand name
- Ondansetron
- Generic name
- Ondansetron
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077535
- Marketed since
- June 25, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin-3 Receptor Antagonist
Active ingredients
- Ondansetron Hydrochloride 4 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68462-105-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-105-30) | Jun 25, 2007 |
| 68462-105-33 | 1 BLISTER PACK in 1 CARTON (68462-105-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK | Jun 25, 2007 |
Recalls mentioning this NDC
- D-0246-2026 Jan 7, 2026 · Class II
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…
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