Ondansetron 63304-0459
Product NDC
63304-0459- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 25, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077851
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ondansetron Hydrochloride | 8 mg/1 |
Drug Class
Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (63304-459-30)