NDC 42708-059 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC42708-059
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- QPharma, 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 8 mg/1
Uses, dosage, side effects and warnings for ondansetron hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42708-059-05 sample | 5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05) | Apr 19, 2018 |
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