Fenofibric Acid

Product NDC

0378-2590

11-digit product format

003782590

Labeler code

0378

Product ID

0378-2590_5c506b03-234c-420a-af44-3b08f4f80540

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fenofibric acid

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA200913

Marketing category

ANDA

Marketing start

2013-07-15

Marketing end

2019-05-31

Substance

FENOFIBRIC ACID

Active strength

135 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