CELECOXIB
- Product NDC
- 63629-8156
- 11-digit product format
- 636298156
- Labeler code
- 63629
- Product ID
- 63629-8156_f4995ac3-cbd8-48cc-b796-5277eb394e35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204776
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- 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 |
|---|
| 63629-8156-1 | 63629815601 | 30 CAPSULE in 1 BOTTLE (63629-8156-1) | 30 capsule | 2021-12-23 | 0000-00-00 | No | No | Current |
| 63629-8156-2 | 63629815602 | 90 CAPSULE in 1 BOTTLE (63629-8156-2) | 90 capsule | 2021-12-23 | 0000-00-00 | No | No | Current |