Fenofibric Acid

Product NDC

53489-677

11-digit product format

534890677

Labeler code

53489

Product ID

53489-677_65f745e9-1116-4c2a-9de8-f64fbf92f641

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibric Acid

Dosage form

TABLET

Route

ORAL

Labeler

Mutual Pharmaceutical Company, Inc.

Application

NDA022418

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2009-08-31

Marketing end

0000-00-00

Substance

FENOFIBRIC ACID

Active strength

35 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record