Fenofibrate
- Product NDC
- 50090-7572
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA216798
- Marketing category
- ANDA
- Substance
- FENOFIBRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7572-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7572-0) | 2025-06-05 | | No | Historical |
| 50090-7572-1 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7572-1) | 2025-06-05 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fenofibrate | A-S Medication Solutions | 2025-06-10 | Human Prescription Drug Label | 4 |