NDC 68071-3731
Etodolac 400 mg tablet, film coated, extended release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-271.
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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Etodolac: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA091134
- On the market since
- Feb 15, 2014
- Package NDCs
68071-3731-4- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2024
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