celecoxib
- Product NDC
- 80175-0142
- 11-digit product format
- 801750142
- Labeler code
- 80175
- Product ID
- 80175-0142_bdc0d316-565f-ff37-e053-2995a90a1cba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Central Packaging
- Application
- ANDA204519
- Marketing category
- ANDA
- Marketing start
- 2015-12-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80175-0142-3 | celecoxib | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80175-0142 | CELECOXIB CAPSULE [CENTRAL PACKAGING] | 1 | Legacy NDC, 1 package rows | 20210225_bbf509e1-a8c2-56b8-e053-2995a90ae5c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80175-0142-3 | 80175014203 | 30 CAPSULE in 1 BOTTLE (80175-0142-3) | 30 capsule | 2015-12-01 | 0000-00-00 | No | No | Current |