NDC 70332-320
Etodolac 600 mg tablet, film coated, extended release
On the label: Fusion Pharmaceuticals LLC. It's repackaged: Fusion Pharmaceuticals LLC rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-273.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- California Pharmaceuticals LLC, Camarillo, California, United States · repackages it
Product details
- Generic drug
- Etodolac: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 600 mg
- Approval
- ANDA ANDA091134
- On the market since
- Aug 3, 2017
- Package NDCs
70332-320-0170332-320-02- Official label
- DailyMed (National Library of Medicine), updated Nov 3, 2017
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