Ondansetron 61919-0565
Product NDC
61919-0565- Manufacturer
- Direct_rx
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA078539
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ondansetron Hydrochloride | 4 mg/1 |
Drug Class
Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)
45 TABLET, FILM COATED in 1 BOTTLE (61919-565-45)