Ondansetron Hydrochloride 65862-0189
Product NDC
65862-0189- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA078539
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ondansetron Hydrochloride | 24 mg/1 |
Drug Class
Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]
Packaging Options(1)
1 BLISTER PACK in 1 CARTON (65862-189-11) / 1 TABLET, FILM COATED in 1 BLISTER PACK