NDC 21695-835
Ondansetron Hydrochloride 8 mg tablet, film coated
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-131.
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 |
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated
- Strength
- 8 mg
- Approval
- ANDA ANDA077050
- On the market since
- Jun 25, 2007
- Package NDCs
21695-835-30- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2010
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