High Outlier
Strength
135 mg/1
Manufacturer
Amneal Pharmaceuticals of New York LLCNDC
00115155510
Classification
Generic
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FENOFIBRIC ACIDApproval Type
Authorized Generic (NDA)
FDA Application
NDA022224On Market Since
9/12/2016
Pharmacological Classes
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