Celecoxib
- Product NDC
- 59762-1518
- 11-digit product format
- 597621518
- Labeler code
- 59762
- Product ID
- 59762-1518_094be167-4b68-4dd0-b996-8802dadf1fc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA020998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-12-10
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 400 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59762-1518 | CELECOXIB CAPSULE [MYLAN PHARMACEUTICALS INC.] | 11 | Legacy NDC | 20250502_12c2b345-bf1c-4661-85a8-257c4af2bda5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-1518-2 | 59762151802 | 60 CAPSULE in 1 BOTTLE (59762-1518-2) | 60 capsule | 2014-12-10 | 0000-00-00 | No | No | Current |