Fenofibrate
- Product NDC
- 50090-7242
- 11-digit product format
- 500907242
- Labeler code
- 50090
- Product ID
- 50090-7242_535158b2-b62b-4905-a6f9-1412e3ed4eaa
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U202363UOS | FENOFIBRATE | 49562-28-9 | FENOFIBRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7242-0 | 50090724200 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7242-0) | 2024-09-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fenofibrate | A-S Medication Solutions | 2024-10-23 | HUMAN PRESCRIPTION DRUG LABEL | 7 |