Celecoxib
- Product NDC
- 80425-0038
- 11-digit product format
- 804250038
- Labeler code
- 80425
- Product ID
- 80425-0038_ed0c24e8-a070-d14c-e053-2995a90ae308
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- NDA020998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-12-10
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80425-0038-1 | 80425003801 | 30 CAPSULE in 1 BOTTLE (80425-0038-1) | 30 capsule | 2014-12-10 | 0000-00-00 | No | No | Current |
| 80425-0038-2 | 80425003802 | 60 CAPSULE in 1 BOTTLE (80425-0038-2) | 60 capsule | 2014-12-10 | 0000-00-00 | No | No | Current |