Celecoxib 200 mg
- Product NDC
- 68788-8969
- 11-digit product format
- 687888969
- Labeler code
- 68788
- Product ID
- 68788-8969_e399d4db-267a-4566-a089-ccb6d98894c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CELECOXIB
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA204519
- Marketing category
- ANDA
- Marketing start
- 2016-01-08
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record