CELECOXIB
- Product NDC
- 50090-2394
- 11-digit product format
- 500902394
- Labeler code
- 50090
- Product ID
- 50090-2394_fdad1520-8118-49c9-a340-ac3b2ae522b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CELECOXIB
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record