Fenofibrate
- Product NDC
- 50090-6934
- 11-digit product format
- 500906934
- Labeler code
- 50090
- Product ID
- 50090-6934_526eebd5-75f5-4f7f-9f33-712872ee1a9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202856
- Marketing category
- ANDA
- Marketing start
- 2013-05-14
- Substance
- FENOFIBRATE
- Active strength
- 145 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fenofibrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FENOFIBRATE | 145 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U202363UOS |
| Rxcui | 477560 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6934-0 | Fenofibrate | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6934 | FENOFIBRATE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, 1 package rows | 20240229_dd98e467-ecb3-463c-81d8-8b4d89159ab0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6934-0 | 50090693400 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-6934-0) | 2023-12-14 | No | No | Current |