CELECOXIB
- Product NDC
- 70518-2748
- 11-digit product format
- 705182748
- Labeler code
- 70518
- Product ID
- 70518-2748_cd8c5ab8-144d-d3f6-e053-2995a90a9473
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204776
- Marketing category
- ANDA
- Marketing start
- 2020-05-19
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2748-0 | 70518274800 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2748-0) | 90 capsule | 2020-05-19 | 0000-00-00 | No | No | Current |