celecoxib
- Product NDC
- 70934-220
- 11-digit product format
- 709340220
- Labeler code
- 70934
- Product ID
- 70934-220_b8161f1c-1fd9-5d74-e053-2a95a90a76dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA204590
- Marketing category
- ANDA
- Marketing start
- 2019-01-04
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-220-30 | 70934022030 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-220-30) | 30 capsule | 2019-01-04 | 0000-00-00 | No | No | Current |