Fenofibrate
- Product NDC
- 50090-6934
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202856
- Marketing category
- ANDA
- Substance
- FENOFIBRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6934-0 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-6934-0) | 2023-12-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fenofibrate | A-S Medication Solutions | 2024-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 6 |