NDC 71205-713
Ondansetron 8 mg tablet, orally disintegrating
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-078.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA090469
- On the market since
- Apr 12, 2010
- Package NDCs
71205-713-1071205-713-2071205-713-3071205-713-6071205-713-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?