NDC 51655-016 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-016
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
- August 8, 2022
- Listing expires
- December 31, 2027
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 51655-016-27 | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27) | Sep 16, 2022 |
| 51655-016-53 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53) | Sep 16, 2022 |
| 51655-016-54 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54) | Aug 8, 2022 |
| 51655-016-87 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87) | Sep 21, 2022 |
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