CELECOXIB
- Product NDC
- 71335-0450
- 11-digit product format
- 713350450
- Labeler code
- 71335
- Product ID
- 71335-0450_6793a756-1df6-46da-8d2f-1abe4ec734a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CELECOXIB
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207446
- Marketing category
- ANDA
- Marketing start
- 2015-09-23
- 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