FENOFIBRATE
- Product NDC
- 50090-1274
- 11-digit product format
- 500901274
- Labeler code
- 50090
- Product ID
- 50090-1274_bc5efb23-102b-4593-b11d-b23de2d63539
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076509
- Marketing category
- ANDA
- Marketing start
- 2010-02-01
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-1274-0 | FENOFIBRATE | 30 in 1 BOTTLE | TABLET | 30 | | 15 |
| 50090-1274-1 | FENOFIBRATE | 90 in 1 BOTTLE | TABLET | 90 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1274 | FENOFIBRATE TABLET [A-S MEDICATION SOLUTIONS] | 15 | Legacy NDC, 2 package rows | 20210416_9ef583a4-9242-4758-a585-401a83df9e6f.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 |
|---|
| 50090-1274-0 | 50090127400 | 30 TABLET in 1 BOTTLE (50090-1274-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1274-1 | 50090127401 | 90 TABLET in 1 BOTTLE (50090-1274-1) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |