celecoxib
- Product NDC
- 70518-1650
- 11-digit product format
- 705181650
- Labeler code
- 70518
- Product ID
- 70518-1650_961a53c8-8bfd-2d44-e053-2995a90a921f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204590
- Marketing category
- ANDA
- Marketing start
- 2018-11-08
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1650 | CELECOXIB CAPSULE [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250227_aa08864f-f681-4c81-9248-d9b4c45480a7.zip |