NDC 62756-130 – Ondansetron hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-130
Product details
- Brand name
- Ondansetron hydrochloride
- Generic name
- Ondansetron hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077050
- Marketed since
- June 25, 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 hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-130-01 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-130-01) | Jun 25, 2007 |
| 62756-130-02 | 10 BLISTER PACK in 1 DOSE PACK (62756-130-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jun 25, 2007 |
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