FENOFIBRATE
- Product NDC
- 50090-6974
- 11-digit product format
- 500906974
- Labeler code
- 50090
- Product ID
- 50090-6974_ceae8452-995f-4005-b8a5-b482b47ca580
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076509
- Marketing category
- ANDA
- Marketing start
- 2022-06-22
- Substance
- FENOFIBRATE
- Active strength
- 160 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6974-0 | 50090697400 | 90 TABLET in 1 BOTTLE (50090-6974-0) | 90 tablet | 2023-12-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FENOFIBRATE | A-S Medication Solutions | 2023-12-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |