NDC 67046-1029
Ondansetron Hydrochloride 4 mg tablet, film coated
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-075.
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
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated
- Strength
- 4 mg
- Approval
- ANDA ANDA078539
- On the market since
- Nov 11, 2024
- Package NDCs
67046-1029-3- Official label
- DailyMed (National Library of Medicine), updated Nov 11, 2024
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