NDC 51655-913
Ondansetron 4 mg tablet, orally disintegrating
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-077.
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
- Northwind Health Company, LLC, Indianapolis, IN, United States · relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA090469
- On the market since
- Jan 22, 2021
- Package NDCs
51655-913-2051655-913-5351655-913-54- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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