Ondansetron 51662-1539
Product NDC
51662-1539- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 6, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA076183
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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(1)
4 BLISTER PACK in 1 BAG (51662-1539-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK