NDC 70518-2233
Celecoxib 200 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Cipla USA., Inc.'s NDC 69097-421.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Indore, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 17, 2023 · 6 inspections, 1 with FDA action |
| Cipla Limited | Pune, India | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyMay 8, 2024 · 7 inspections |
Product details
- Generic drug
- Celecoxib: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA207446
- On the market since
- Jul 24, 2019
- Package NDCs
70518-2233-070518-2233-170518-2233-2- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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