celecoxib
- Product NDC
- 55700-607
- 11-digit product format
- 557000607
- Labeler code
- 55700
- Product ID
- 55700-607_8a368941-8a2a-43d5-a6b1-f48e2111f9f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA204590
- Marketing category
- ANDA
- Marketing start
- 2018-04-20
- 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 |
|---|
| 55700-607-14 | 55700060714 | 14 CAPSULE in 1 BOTTLE (55700-607-14) | 14 capsule | 2022-02-16 | 0000-00-00 | No | No | Current |
| 55700-607-30 | 55700060730 | 30 CAPSULE in 1 BOTTLE (55700-607-30) | 30 capsule | 2018-04-20 | 0000-00-00 | No | No | Current |
| 55700-607-60 | 55700060760 | 60 CAPSULE in 1 BOTTLE (55700-607-60) | 60 capsule | 2018-04-20 | 0000-00-00 | No | No | Current |