celecoxib
- Product NDC
- 70518-1346
- 11-digit product format
- 705181346
- Labeler code
- 70518
- Product ID
- 70518-1346_e8b908b5-dbaf-1e8a-e053-2995a90a185c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204590
- Marketing category
- ANDA
- Marketing start
- 2018-08-06
- 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 |
|---|
| 70518-1346-0 | 70518134600 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-1346-0) | 30 capsule | 2018-08-06 | 0000-00-00 | No | No | Current |
| 70518-1346-1 | 70518134601 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1346-1) | 90 capsule | 2019-04-15 | 0000-00-00 | No | No | Current |
| 70518-1346-2 | 70518134602 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-1346-2) | 60 capsule | 2019-10-16 | 0000-00-00 | No | No | Current |