NDC 68788-9402 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-9402
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- June 12, 2012
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-9402-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-9402-1) | Jun 12, 2012 |
| 68788-9402-2 | 12 TABLET, FILM COATED in 1 BOTTLE (68788-9402-2) | Jun 23, 2017 |
| 68788-9402-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9402-3) | Jun 12, 2012 |
| 68788-9402-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-9402-5) | Jun 23, 2017 |
| 68788-9402-6 | 6 TABLET, FILM COATED in 1 BOTTLE (68788-9402-6) | Jun 23, 2017 |
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