Ondansetron Hydrochloride 60760-0636
Product NDC
60760-0636- Manufacturer
- St. Mary's Medical Park Pharmacy
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2007
- 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(3)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10)
16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20)