Celecoxib
- Product NDC
- 68071-4476
- 11-digit product format
- 680714476
- Labeler code
- 68071
- Product ID
- 68071-4476_c250f866-dc3c-1c29-e053-2a95a90ae9c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204519
- Marketing category
- ANDA
- Marketing start
- 2015-12-01
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 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 |
|---|
| 68071-4476-3 | 68071447603 | 30 CAPSULE in 1 BOTTLE (68071-4476-3) | 30 capsule | 2018-06-21 | 0000-00-00 | No | No | Current |
| 68071-4476-7 | 68071447607 | 7 CAPSULE in 1 BOTTLE (68071-4476-7) | 7 capsule | 2018-06-21 | 0000-00-00 | No | No | Current |