Celecoxib
- Product NDC
- 0093-7165
- 11-digit product format
- 000937165
- Labeler code
- 0093
- Product ID
- 0093-7165_6fff9b26-6a00-4968-b7c8-d7b33f6915f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076898
- Marketing category
- ANDA
- Marketing start
- 2014-12-10
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 100 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7165-01 | 00093716501 | 100 CAPSULE in 1 BOTTLE (0093-7165-01) | 100 capsule | 2014-12-10 | 0000-00-00 | No | No | Current |
| 0093-7165-05 | 00093716505 | 500 CAPSULE in 1 BOTTLE (0093-7165-05) | 500 capsule | 2014-12-10 | 0000-00-00 | No | No | Current |