Fenofibrate 68071-4991
Product NDC
68071-4991- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 20, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210138
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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 in 1 BOTTLE (68071-4991-9)