NDC 68071-2053 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-2053
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- NuCare Pharmaceuticals,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 |
|---|---|---|
| 68071-2053-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-2053-1) | Nov 16, 2020 |
| 68071-2053-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-2053-2) | Jan 14, 2025 |
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