NDC 85509-1237
Celecoxib 100 mg capsule
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Pharmaceutical Associates, Inc.'s NDC 75834-237.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it | Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Celecoxib: every company that makes it
- Form
- capsule, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA210628
- On the market since
- Sep 3, 2020
- Package NDCs
85509-1237-185509-1237-385509-1237-685509-1237-9- Official label
- DailyMed (National Library of Medicine), updated Aug 3, 2025
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