NDC 70518-4145 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4145
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
- July 18, 2024
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4145-0 | 16 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-0) | Jul 18, 2024 |
| 70518-4145-1 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-1) | Jul 18, 2024 |
| 70518-4145-2 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-2) | Dec 20, 2024 |
| 70518-4145-3 | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4145-3) | Apr 2, 2025 |
| 70518-4145-4 | 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4145-4) | Sep 5, 2026 |
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