Fenofibrate

Product NDC

68071-2021

11-digit product format

680712021

Labeler code

68071

Product ID

68071-2021_48aa7ef3-9f86-2a08-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA204019

Marketing category

ANDA

Marketing start

2015-11-23

Marketing end

0000-00-00

Substance

FENOFIBRATE

Active strength

160 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