FIBRICOR - 13310-101-05 - (Fenofibric Acid)

Alphabetical Index


Drug Information of FIBRICOR

Product NDC: 13310-101
Proprietary Name: FIBRICOR
Non Proprietary Name: Fenofibric Acid
Active Ingredient(s): 35    mg/1 & nbsp;   Fenofibric Acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FIBRICOR

Product NDC: 13310-101
Labeler Name: AR Scientific, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022418
Marketing Category: NDA
Start Marketing Date: 20090814

Package Information of FIBRICOR

Package NDC: 13310-101-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (13310-101-05)

NDC Information of FIBRICOR

NDC Code 13310-101-05
Proprietary Name FIBRICOR
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (13310-101-05)
Product NDC 13310-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibric Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090814
Marketing Category Name NDA
Labeler Name AR Scientific, Inc.
Substance Name FENOFIBRIC ACID
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC]

Complete Information of FIBRICOR


General Information