Fenofibrate

Product NDC

63629-6459

11-digit product format

636296459

Labeler code

63629

Product ID

63629-6459_191438b5-eba1-4aea-9d93-0006f3e8658a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

NDA021656

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-02-09

Marketing end

0000-00-00

Substance

FENOFIBRATE

Active strength

145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record