NDC 68071-5230
ondansetron 8 mg tablet, orally disintegrating
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-356.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA077557
- On the market since
- Aug 2, 2007
- Package NDCs
68071-5230-1- Official label
- DailyMed (National Library of Medicine), updated Jun 20, 2024
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