NDC 61919-465
Ondansetron Hydrochloride 8 mg tablet, film coated
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-459.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Natco Pharma Limited | Rangareddy, India | Makes it | Problems found, fixed voluntarilyJun 19, 2025 · 7 inspections |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated
- Strength
- 8 mg
- Approval
- ANDA ANDA077851
- On the market since
- Jan 1, 2014
- Package NDCs
61919-465-0661919-465-1061919-465-3061919-465-60- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2016
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?