NDC 68071-2733
Celecoxib 200 mg capsule
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-158.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Celecoxib: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA205129
- On the market since
- Dec 3, 2020
- Package NDCs
68071-2733-068071-2733-368071-2733-6- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2024
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