Strength
43 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
63304044330
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
FENOFIBRATEApproval Type
Generic (ANDA)
FDA Application
ANDA201748On Market Since
3/2/2015
Pharmacological Classes
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