Celecoxib
- Product NDC
- 10544-917
- 11-digit product format
- 105440917
- Labeler code
- 10544
- Product ID
- 10544-917_17125c3e-c283-274c-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- NDA020998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-05-19
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10544-917-14 | Celecoxib | 14 in 1 BOTTLE | CAPSULE | 14 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-917 | CELECOXIB CAPSULE [BLENHEIM PHARMACAL, INC.] | 2 | Legacy NDC, 1 package rows | 20150527_167291dc-78ea-1346-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-917-14 | 10544091714 | 14 in 1 BOTTLE | Historical |