Ondansetron Hydrochloride 70518-3511
Product NDC
70518-3511- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 6, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA078539
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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(2)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1)