Fenofibrate 63304-0443
Product NDC
63304-0443- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 2, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA201748
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fenofibrate | 43 mg/1 |
Drug Class
Peroxisome Proliferator Receptor alpha Agonist [EPC]Peroxisome Proliferator Receptor alpha Agonist [EPC]
Packaging Options(2)
500 CAPSULE in 1 BOTTLE (63304-443-05)
30 CAPSULE in 1 BOTTLE (63304-443-30)