Ondansetron Hydrochloride 85509-1075
Product NDC
85509-1075- Manufacturer
- Phoenix Rx Llc
- 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 | 4 mg/1 |
Drug Class
Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]
Packaging Options(6)
10 TABLET, FILM COATED in 1 BOTTLE (85509-1075-1)
20 TABLET, FILM COATED in 1 BOTTLE (85509-1075-2)
30 TABLET, FILM COATED in 1 BOTTLE (85509-1075-3)
12 TABLET, FILM COATED in 1 BOTTLE (85509-1075-4)
15 TABLET, FILM COATED in 1 BOTTLE (85509-1075-5)
60 TABLET, FILM COATED in 1 BOTTLE (85509-1075-6)