FENOFIBRATE

Product NDC

0179-0103

11-digit product format

001790103

Labeler code

0179

Product ID

0179-0103_7baea303-1390-5a69-e053-2991aa0a5f54

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FENOFIBRATE

Dosage form

TABLET

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA076509

Marketing category

ANDA

Marketing start

2011-08-03

Marketing end

2020-06-30

Substance

FENOFIBRATE

Active strength

54 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record