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
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 |
|---|
| 50090-6120-0 | 50090612000 | 90 CAPSULE in 1 BOTTLE (50090-6120-0) | 90 capsule | 2022-09-30 | No | No | Historical |