NDC 70332-310
Oxaprozin 600 mg tablet, film coated
On the label: Fusion Pharmaceuticals LLC. It's repackaged: Fusion Pharmaceuticals LLC rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-170.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- California Pharmaceuticals LLC, Camarillo, California, United States · repackages it
Product details
- Generic drug
- Oxaprozin: every company that makes it
- Form
- tablet, film coated
- Strength
- 600 mg
- Approval
- ANDA ANDA075855
- On the market since
- Jul 1, 2017
- Package NDCs
70332-310-0170332-310-02- Official label
- DailyMed (National Library of Medicine), updated Nov 3, 2017
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