Home > National Drug Code (NDC) > Fenofibrate

Fenofibrate - 68084-636-25 - (Fenofibrate)

Alphabetical Index


Drug Information of Fenofibrate

Product NDC: 68084-636
Proprietary Name: Fenofibrate
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 145    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 68084-636
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090856
Marketing Category: ANDA
Start Marketing Date: 20130206

Package Information of Fenofibrate

Package NDC: 68084-636-25
Package Description: 5 BLISTER PACK in 1 CARTON (68084-636-25) > 6 TABLET in 1 BLISTER PACK (68084-636-95)

NDC Information of Fenofibrate

NDC Code 68084-636-25
Proprietary Name Fenofibrate
Package Description 5 BLISTER PACK in 1 CARTON (68084-636-25) > 6 TABLET in 1 BLISTER PACK (68084-636-95)
Product NDC 68084-636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130206
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name FENOFIBRATE
Strength Number 145
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 Fenofibrate


General Information