NDC 50090-4671 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-4671
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- July 31, 2007
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 50090-4671-0 | 4 TABLET, FILM COATED in 1 BOTTLE (50090-4671-0) | Nov 1, 2019 |
| 50090-4671-1 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-4671-1) | Nov 1, 2019 |
| 50090-4671-2 | 3 TABLET, FILM COATED in 1 BOTTLE (50090-4671-2) | Nov 1, 2019 |
| 50090-4671-3 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4671-3) | Nov 1, 2019 |
| 50090-4671-4 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-4671-4) | Nov 1, 2019 |
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