Fenoglide - 54868-6118-0 - (fenofibrate)

Alphabetical Index


Drug Information of Fenoglide

Product NDC: 54868-6118
Proprietary Name: Fenoglide
Non Proprietary Name: fenofibrate
Active Ingredient(s): 120    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fenoglide

Product NDC: 54868-6118
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022118
Marketing Category: NDA
Start Marketing Date: 20100428

Package Information of Fenoglide

Package NDC: 54868-6118-0
Package Description: 30 TABLET in 1 BOTTLE (54868-6118-0)

NDC Information of Fenoglide

NDC Code 54868-6118-0
Proprietary Name Fenoglide
Package Description 30 TABLET in 1 BOTTLE (54868-6118-0)
Product NDC 54868-6118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100428
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name FENOFIBRATE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Complete Information of Fenoglide


General Information