Fenofibrate
- Product NDC
- 50090-3904
- 11-digit product format
- 500903904
- Labeler code
- 50090
- Product ID
- 50090-3904_16d95c03-1d0d-45a3-aa1c-39ddfc74faf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090856
- Marketing category
- ANDA
- Marketing start
- 2012-11-19
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-3904-0 | Fenofibrate | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3904 | FENOFIBRATE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20200121_2e82e604-feec-4ac7-ab62-28f602d4d0d1.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 |
|---|
| 50090-3904-0 | 50090390400 | 90 TABLET in 1 BOTTLE (50090-3904-0) | 90 tablet | 2018-12-05 | 0000-00-00 | No | No | Current |