NDC 85766-053 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC85766-053
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Sportpharm LLC
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 85766-053-05 | 5 TABLET, FILM COATED in 1 BOTTLE (85766-053-05) | Oct 1, 2025 |
| 85766-053-10 | 10 TABLET, FILM COATED in 1 BOTTLE (85766-053-10) | Oct 1, 2025 |
| 85766-053-14 | 14 TABLET, FILM COATED in 1 BOTTLE (85766-053-14) | Oct 1, 2025 |
| 85766-053-20 | 20 TABLET, FILM COATED in 1 BOTTLE (85766-053-20) | Oct 1, 2025 |
| 85766-053-24 | 24 TABLET, FILM COATED in 1 BOTTLE (85766-053-24) | Oct 1, 2025 |
| 85766-053-30 | 30 TABLET, FILM COATED in 1 BOTTLE (85766-053-30) | Oct 1, 2025 |
| 85766-053-60 | 60 TABLET, FILM COATED in 1 BOTTLE (85766-053-60) | Oct 1, 2025 |
| 85766-053-90 | 90 TABLET, FILM COATED in 1 BOTTLE (85766-053-90) | Oct 1, 2025 |
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