Fenofibrate

Product NDC

68071-4088

11-digit product format

680714088

Labeler code

68071

Product ID

68071-4088_5900270c-1926-79c5-e053-2a91aa0ac375

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fenofibrate

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA207378

Marketing category

ANDA

Marketing start

2017-03-30

Marketing end

0000-00-00

Substance

FENOFIBRATE

Active strength

134 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record