CELECOXIB
- Product NDC
- 70934-978
- 11-digit product format
- 709340978
- Labeler code
- 70934
- Product ID
- 70934-978_f1628c66-564e-fa92-e053-2995a90a601f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CELECOXIB
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA207446
- Marketing category
- ANDA
- Marketing start
- 2022-06-09
- Marketing end
- 2023-11-30
- 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 |
|---|
| 70934-978-30 | 70934097830 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-978-30) | 30 capsule | 2022-06-09 | 0000-00-00 | No | No | Current |