NDC 51655-415 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-415
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- December 7, 2017
- Listing expires
- December 31, 2027
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 51655-415-04 | 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04) | Apr 12, 2018 |
| 51655-415-43 | 3 TABLET, FILM COATED in 1 BOTTLE (51655-415-43) | Dec 28, 2017 |
| 51655-415-53 | 10 TABLET, FILM COATED in 1 BOTTLE (51655-415-53) | Apr 24, 2018 |
| 51655-415-54 | 15 TABLET, FILM COATED in 1 BOTTLE (51655-415-54) | Dec 28, 2017 |
| 51655-415-55 | 5 TABLET, FILM COATED in 1 BOTTLE (51655-415-55) | Dec 7, 2017 |
| 51655-415-87 | 6 TABLET, FILM COATED in 1 BOTTLE (51655-415-87) | Oct 24, 2018 |
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