NDC 51662-1678 – Ondansetron
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC51662-1678
Product details
- Brand name
- Ondansetron
- Generic name
- Ondansetron
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076183
- Marketed since
- December 26, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin-3 Receptor Antagonist
Active ingredients
- Ondansetron Hydrochloride 4 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51662-1678-1 | 30 TABLET, FILM COATED in 1 BOTTLE (51662-1678-1) | Dec 26, 2006 |
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