fenofibrate
- Product NDC
- 50090-6120
- 11-digit product format
- 500906120
- Labeler code
- 50090
- Product ID
- 50090-6120_1fb9e6f1-a9ad-4138-ae2e-09f0258bf929
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205566
- Marketing category
- ANDA
- Marketing start
- 2017-04-07
- Substance
- FENOFIBRATE
- Active strength
- 134 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 | 134 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U202363UOS |
| Rxcui | 310288 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6120-0 | fenofibrate | 90 in 1 BOTTLE | CAPSULE | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6120 | FENOFIBRATE CAPSULE [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231102_9d284236-c788-4e9e-8573-4d119e45d3b9.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 |
|---|
| 50090-6120-0 | 50090612000 | 90 CAPSULE in 1 BOTTLE (50090-6120-0) | 90 capsule | 2022-09-30 | 0000-00-00 | No | No | Current |