Fenofibrate

Product NDC

55700-319

11-digit product format

557000319

Labeler code

55700

Product ID

55700-319_31dc737d-3e32-4127-8105-3cf6daa12212

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

NDA021656

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2004-11-05

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