Fenofibrate 63304-0449
Product NDC
63304-0449- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA200884
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fenofibrate | 145 mg/1 |
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]Peroxisome Proliferator Receptor alpha Agonist [EPC]
Packaging Options(3)
500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)
30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30)
90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)