Fenofibrate 69315-0290
Product NDC
69315-0290- Manufacturer
- Leading Pharma, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 20, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA210606
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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(2)
500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
90 TABLET, FILM COATED in 1 BOTTLE (69315-290-09)