fenofibrate

Product NDC

50090-2692

11-digit product format

500902692

Labeler code

50090

Product ID

50090-2692_4219c298-20f7-4c6a-84ca-6aec63612e84

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fenofibrate

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA090715

Marketing category

ANDA

Marketing start

2014-08-13

Marketing end

0000-00-00

Substance

FENOFIBRATE

Active strength

48 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