NDC 85509-1076
Ondansetron Hydrochloride 8 mg tablet, film coated
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC 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
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels 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
- Jul 31, 2007
- Package NDCs
85509-1076-185509-1076-285509-1076-385509-1076-585509-1076-6- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?