Fenofibrate

Product NDC

50090-2857

11-digit product format

500902857

Labeler code

50090

Product ID

50090-2857_368b6f01-0cc4-4f43-957c-967524ea3e6d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA021656

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-02-09

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