NDC 70518-3511 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3511
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- September 6, 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3511-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0) | Sep 6, 2022 |
| 70518-3511-1 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1) | Jul 2, 2025 |
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