Fenofibrate
- Product NDC
- 50090-3056
- 11-digit product format
- 500903056
- Labeler code
- 50090
- Product ID
- 50090-3056_ada831fc-d14a-4b44-824f-6e6dac65b073
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204598
- Marketing category
- ANDA
- Marketing start
- 2016-07-14
- Substance
- FENOFIBRATE
- Active strength
- 48 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fenofibrate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FENOFIBRATE | 48 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U202363UOS |
| Rxcui | 477560, 477562 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3056-0 | Fenofibrate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3056 | FENOFIBRATE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 13 | Current NDC, Legacy NDC, 1 package rows | 20241030_d9c60b43-dc61-4976-b31f-09c8f8a33138.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-3056-0 | 50090305600 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3056-0) | 2017-06-14 | No | No | Historical |