NDC 65862-189 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 24 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-189
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- 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 24 mg/1
Uses, dosage, side effects and warnings for Ondansetron hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65862-189-11 | 1 BLISTER PACK in 1 CARTON (65862-189-11) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Jul 31, 2007 |
Recalls mentioning this NDC
- D-1103-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse
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