LIPOFEN - 66869-137-30 - (fenofibrate)

Alphabetical Index


Drug Information of LIPOFEN

Product NDC: 66869-137
Proprietary Name: LIPOFEN
Non Proprietary Name: fenofibrate
Active Ingredient(s): 50    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of LIPOFEN

Product NDC: 66869-137
Labeler Name: Kowa Pharmaceuticals America Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021612
Marketing Category: NDA
Start Marketing Date: 20071001

Package Information of LIPOFEN

Package NDC: 66869-137-30
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (66869-137-30)

NDC Information of LIPOFEN

NDC Code 66869-137-30
Proprietary Name LIPOFEN
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (66869-137-30)
Product NDC 66869-137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20071001
Marketing Category Name NDA
Labeler Name Kowa Pharmaceuticals America Inc.
Substance Name FENOFIBRATE
Strength Number 50
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 LIPOFEN


General Information