FENOFIBRATE

Product NDC

69597-346

11-digit product format

695970346

Labeler code

69597

Product ID

69597-346_557013b8-e189-4b6a-b2fd-620194917a54

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FENOFIBRATE

Dosage form

TABLET

Route

ORAL

Labeler

Basiem

Application

NDA021350

Marketing category

NDA

Marketing start

2019-03-19

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