NDC 70518-1585 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-1585
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
- October 24, 2018
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1585-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-0) | Oct 24, 2018 |
| 70518-1585-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-1) | Jan 6, 2021 |
| 70518-1585-6 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6) | Oct 1, 2025 |
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