NDC 71205-744 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-744
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Proficient Rx LP
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-744-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-744-10) | Jan 16, 2023 |
| 71205-744-12 | 12 TABLET, FILM COATED in 1 BOTTLE (71205-744-12) | Jun 13, 2023 |
| 71205-744-15 | 15 TABLET, FILM COATED in 1 BOTTLE (71205-744-15) | Jan 16, 2023 |
| 71205-744-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-744-20) | Jan 16, 2023 |
| 71205-744-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-744-30) | Jan 16, 2023 |
| 71205-744-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-744-60) | Jan 16, 2023 |
| 71205-744-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-744-90) | Jan 16, 2023 |
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