NDC 70332-311
Oxaprozin 600 mg tablet
On the label: Fusion Pharmaceuticals LLC. It's repackaged: Fusion Pharmaceuticals LLC rebottles it from Amneal Pharmaceuticals's NDC 69238-1120.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | No problems foundJul 19, 2024 · 6 inspections |
Repackaging site
- California Pharmaceuticals LLC, Camarillo, California, United States · repackages it
Product details
- Generic drug
- Oxaprozin: every company that makes it
- Form
- tablet
- Strength
- 600 mg
- Approval
- ANDA ANDA208633
- On the market since
- Jan 2, 2018
- Package NDCs
70332-311-02- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2018
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