NDC 55111-155 – Ondansetron hydrochloride
Ondansetron Hydrochloride 16 mg/1 · Tablet, Film Coated · Oral
Product NDC55111-155
Product details
- Brand name
- Ondansetron hydrochloride
- Generic name
- Ondansetron hydrochloride
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076183
- Marketed since
- December 26, 2006
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin-3 Receptor Antagonist
Active ingredients
- Ondansetron Hydrochloride 16 mg/1
Uses, dosage, side effects and warnings for Ondansetron hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 55111-155-05 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-155-05) | Dec 26, 2006 |
| 55111-155-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55111-155-30) | Dec 26, 2006 |
| 55111-155-78 | 10 BLISTER PACK in 1 CARTON (55111-155-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-155-79) | Dec 26, 2006 |
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