NDC 50090-6342 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-6342
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, 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 50090-6342-0 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-6342-0) | Jan 23, 2023 |
| 50090-6342-1 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-6342-1) | Jan 23, 2023 |
| 50090-6342-2 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-6342-2) | Jan 23, 2023 |
| 50090-6342-4 | 3 TABLET, FILM COATED in 1 BOTTLE (50090-6342-4) | Jan 23, 2023 |
| 50090-6342-5 | 12 TABLET, FILM COATED in 1 BOTTLE (50090-6342-5) | Jan 23, 2023 |
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