NDC 85509-1076 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1076
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- PHOENIX RX LLC
- 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 8 mg/1
Uses, dosage, side effects and warnings for Ondansetron hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 85509-1076-1 | 10 TABLET, FILM COATED in 1 BOTTLE (85509-1076-1) | Jul 31, 2025 |
| 85509-1076-2 | 20 TABLET, FILM COATED in 1 BOTTLE (85509-1076-2) | Jul 31, 2025 |
| 85509-1076-3 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1076-3) | Jul 31, 2025 |
| 85509-1076-5 | 15 TABLET, FILM COATED in 1 BOTTLE (85509-1076-5) | Jul 31, 2025 |
| 85509-1076-6 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1076-6) | Jul 31, 2025 |
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