Celecoxib
- Product NDC
- 71335-0597
- 11-digit product format
- 713350597
- Labeler code
- 71335
- Product ID
- 71335-0597_7b5fa1a4-358d-4c9a-b575-61f2bdda5ca4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200562
- Marketing category
- ANDA
- Marketing start
- 2015-03-12
- 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