Fenofibrate 68071-3542
Product NDC
68071-3542- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 27, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA216798
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fenofibrate | 160 mg/1 |
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]Peroxisome Proliferator Receptor alpha Agonist [EPC]
Packaging Options(1)
90 TABLET, FILM COATED in 1 BOTTLE (68071-3542-9)