Celecoxib
- Product NDC
- 81288-020
- 11-digit product format
- 812880020
- Labeler code
- 81288
- Product ID
- 81288-020_9dca0e35-a3f7-499a-a256-ad4de9a78812
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- EMC PHARMA, LLC
- Application
- ANDA211412
- Marketing category
- ANDA
- Marketing start
- 2022-07-18
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 50 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 |
|---|
| 81288-020-10 | 81288002010 | 60 CAPSULE in 1 BOTTLE (81288-020-10) | 60 capsule | 2022-07-18 | 0000-00-00 | No | No | Current |
| 81288-020-20 | 81288002020 | 100 CAPSULE in 1 BOTTLE (81288-020-20) | 100 capsule | 2022-07-18 | 0000-00-00 | No | No | Current |
| 81288-020-30 | 81288002030 | 500 CAPSULE in 1 BOTTLE (81288-020-30) | 500 capsule | 2022-07-18 | 0000-00-00 | No | No | Current |