Fenofibrate

Product NDC

0378-6089

11-digit product format

003786089

Labeler code

0378

Product ID

0378-6089_9c393afd-652f-44b8-a0e1-7c03d7427f75

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fenofibrate

Dosage form

CAPSULE

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA202579

Marketing category

ANDA

Marketing start

2013-02-22

Marketing end

2020-05-31

Substance

FENOFIBRATE

Active strength

130 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