Fenofibrate

Product NDC

68071-2042

11-digit product format

680712042

Labeler code

68071

Product ID

68071-2042_481f8cd9-8791-017f-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA021656

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-02-09

Marketing end

0000-00-00

Substance

FENOFIBRATE

Active strength

48 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record