NDC 57237-075 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC57237-075
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- July 31, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin-3 Receptor Antagonist
Active ingredients
- Ondansetron Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Ondansetron hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 57237-075-30 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-075-30) | Jul 31, 2007 |
| 57237-075-50 | 500 TABLET, FILM COATED in 1 BOTTLE (57237-075-50) | Oct 4, 2022 |
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