NDC 68788-8651
Ondansetron Hydrochloride 4 mg tablet, film coated
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. 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
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA078539
- On the market since
- Apr 29, 2024
- Package NDCs
68788-8651-168788-8651-268788-8651-368788-8651-568788-8651-6- Official label
- DailyMed (National Library of Medicine), updated Sep 3, 2025
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