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Fenofibrate - 68180-361-02 - (Fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 68180-361
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: 68180-361
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090856
Marketing Category: ANDA
Start Marketing Date: 20120713

Package Information of Fenofibrate

Package NDC: 68180-361-02
Package Description: 500 TABLET in 1 BOTTLE (68180-361-02)

NDC Information of Fenofibrate

NDC Code 68180-361-02
Proprietary Name Fenofibrate
Package Description 500 TABLET in 1 BOTTLE (68180-361-02)
Product NDC 68180-361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120713
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
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