NDC 76420-251
Ondansetron 8 mg tablet, orally disintegrating
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-078.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA090469
- On the market since
- Apr 12, 2010
- Package NDCs
76420-251-0476420-251-0676420-251-1076420-251-2076420-251-30- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2025
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