FENOFIBRATE
- Product NDC
- 71205-666
- 11-digit product format
- 712050666
- Labeler code
- 71205
- Product ID
- 71205-666_26f8f793-fb7a-4327-9441-d8737fe1ff11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA213864
- Marketing category
- ANDA
- Marketing start
- 2020-09-10
- Substance
- FENOFIBRATE
- Active strength
- 54 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 |
|---|
| 71205-666-30 | 71205066630 | 30 TABLET in 1 BOTTLE (71205-666-30) | 30 tablet | 2022-06-01 | No | No | Historical |
| 71205-666-60 | 71205066660 | 60 TABLET in 1 BOTTLE (71205-666-60) | 60 tablet | 2022-06-01 | No | No | Historical |
| 71205-666-90 | 71205066690 | 90 TABLET in 1 BOTTLE (71205-666-90) | 90 tablet | 2022-06-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FENOFIBRATE | Proficient Rx LP | 2022-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |