Fenofibrate
- Product NDC
- 60687-864
- 11-digit product format
- 606870864
- Labeler code
- 60687
- Product ID
- 60687-864_2f0f3dde-ad02-363f-e063-6394a90a1073
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2025-04-19
- 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 |
|---|
| 60687-864-21 | 60687086421 | 30 BLISTER PACK in 1 CARTON (60687-864-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-864-11) | 30 blister pack | 2025-04-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fenofibrate | American Health Packaging | 2025-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |