NDC 80425-0072 – Ondansetron HCL
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0072
Product details
- Brand name
- Ondansetron HCL
- Generic name
- Ondansetron HCL
- Labeler
- Advanced Rx of Tennessee, 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 4 mg/1
Uses, dosage, side effects and warnings for Ondansetron HCL →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0072-1 | 20 TABLET, FILM COATED in 1 BOTTLE (80425-0072-1) | Jul 31, 2007 |
| 80425-0072-2 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0072-2) | Jul 31, 2007 |
| 80425-0072-3 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0072-3) | Jul 31, 2007 |
| 80425-0072-4 | 15 TABLET, FILM COATED in 1 BOTTLE (80425-0072-4) | Jul 31, 2007 |
| 80425-0072-5 | 10 TABLET, FILM COATED in 1 BOTTLE (80425-0072-5) | Jul 31, 2007 |
Other Ondansetron HCL products
- 80425-0074 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Advanced Rx of Tennessee, LLC
- 80425-0075 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Advanced Rx of Tennessee, LLC