Ondansetron Hydrochloride 51655-0933
Product NDC
51655-0933- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 20, 2022
- 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(6)
4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04)
3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53)
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-54)
5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55)
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87)