Celecoxib
- Product NDC
- 0378-7150
- 11-digit product format
- 003787150
- Labeler code
- 0378
- Product ID
- 0378-7150_bf30a30a-9307-4319-a5c2-d0f59dfc546e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA078857
- Marketing category
- ANDA
- Marketing start
- 2014-05-30
- Marketing end
- 2023-05-31
- 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
- 0000-00-00
- 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 |
|---|
| 0378-7150-01 | 00378715001 | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7150-01) | 100 capsule | 2014-05-30 | 0000-00-00 | No | No | Current |
| 0378-7150-05 | 00378715005 | 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-7150-05) | 500 capsule | 2014-05-30 | 0000-00-00 | No | No | Current |