FENOFIBRATE
- Product NDC
- 50090-4031
- 11-digit product format
- 500904031
- Labeler code
- 50090
- Product ID
- 50090-4031_4f3d9bfe-fe00-4bae-92ba-5c3f8e53e686
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208709
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- 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
- 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 |
|---|
| 50090-4031-0 | FENOFIBRATE | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4031 | FENOFIBRATE TABLET [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 1 package rows | 20210417_c870ea48-5dde-4a6f-9ddb-56b494bb2b55.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 |
|---|
| 50090-4031-0 | 50090403100 | 90 TABLET in 1 BOTTLE (50090-4031-0) | 90 tablet | 2019-01-09 | 0000-00-00 | No | No | Current |