Fenofibrate

Product NDC

0093-7755

11-digit product format

000937755

Labeler code

0093

Product ID

0093-7755_ac5ab4b2-199c-b491-0a82-7d07695b6adf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA Inc

Application

NDA021656

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-02-09

Marketing end

2020-07-31

Substance

FENOFIBRATE

Active strength

48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record