Celecoxib
- Product NDC
- 72162-2254
- 11-digit product format
- 721622254
- Labeler code
- 72162
- Product ID
- 72162-2254_3cbd036a-8c83-4794-827c-3ef6d91921d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205129
- Marketing category
- ANDA
- Marketing start
- 2020-12-03
- Substance
- CELECOXIB
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JCX84Q7J1L | CELECOXIB | 169590-42-5 | CELECOXIB |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2254-5 | 72162225405 | 500 CAPSULE in 1 BOTTLE (72162-2254-5) | 500 capsule | 2024-02-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Celecoxib | Bryant Ranch Prepack | 2024-02-23 | HUMAN PRESCRIPTION DRUG LABEL | 100 |