Celecoxib
- Product NDC
- 50436-3984
- 11-digit product format
- 504363984
- Labeler code
- 50436
- Product ID
- 50436-3984_a360f53f-e638-445f-9fe2-9bf11baa7c0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA200562
- Marketing category
- ANDA
- Marketing start
- 2015-03-12
- 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
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 |
|---|
| 50436-3984-1 | Celecoxib | 30 in 1 BOTTLE | CAPSULE | 30 | | 6 |
| 50436-3984-2 | Celecoxib | 60 in 1 BOTTLE | CAPSULE | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3984 | CELECOXIB CAPSULE [UNIT DOSE SERVICES] | 6 | Legacy NDC, 2 package rows | 20221018_298dd3a8-2cec-4260-961a-6294d08eecf7.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 |
|---|
| 50436-3984-1 | 50436398401 | 30 CAPSULE in 1 BOTTLE (50436-3984-1) | 30 capsule | 2016-08-01 | 0000-00-00 | No | No | Current |
| 50436-3984-2 | 50436398402 | 60 CAPSULE in 1 BOTTLE (50436-3984-2) | 60 capsule | 2016-08-01 | 0000-00-00 | No | No | Current |