NDC 45865-943
Celecoxib 200 mg capsule
On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Alembic Pharmaceuticals Inc.'s NDC 62332-142.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
| Alembic Pharmaceuticals Limited | Vadodara, India | Makes it | Problems found, fixed voluntarilyNov 22, 2024 · 1 inspection |
Repackaging site
- Medsource Pharmaceuticals, Rancho Santa Margarita, CA, United States · repackages it
Recalls
- May 9, 2025 · Class II · Alembic Pharmaceuticals Limited
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Lots: Batch 2405014780, Exp. Date: Sep. 30, 2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Celecoxib: every company that makes it
- Form
- capsule
- Strength
- 200 mg
- Approval
- ANDA ANDA204519
- On the market since
- Dec 1, 2015
- Package NDCs
45865-943-30- Official label
- DailyMed (National Library of Medicine), updated Dec 29, 2019
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