NDC 68788-8582
Ondansetron Hydrochloride 8 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 57237-076.
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
- 8 mg
- Approval
- ANDA ANDA078539
- On the market since
- Feb 12, 2024
- Package NDCs
68788-8582-168788-8582-268788-8582-368788-8582-568788-8582-6- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2026
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