Gemfibrozil

Product NDC

50090-2450

11-digit product format

500902450

Labeler code

50090

Product ID

50090-2450_c2b7602c-23a5-431c-ba44-e9ebb2326ae0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gemfibrozil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA202726

Marketing category

ANDA

Marketing start

2015-09-16

Marketing end

0000-00-00

Substance

GEMFIBROZIL

Active strength

600 mg/1

Pharmacologic classes

Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record