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Fenofibrate - 42043-171-09 - (Fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 42043-171
Proprietary Name: Fenofibrate
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 160    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 42043-171
Labeler Name: Karalex Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076520
Marketing Category: ANDA
Start Marketing Date: 20091120

Package Information of Fenofibrate

Package NDC: 42043-171-09
Package Description: 90 TABLET, COATED in 1 BOTTLE (42043-171-09)

NDC Information of Fenofibrate

NDC Code 42043-171-09
Proprietary Name Fenofibrate
Package Description 90 TABLET, COATED in 1 BOTTLE (42043-171-09)
Product NDC 42043-171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20091120
Marketing Category Name ANDA
Labeler Name Karalex Pharma LLC
Substance Name FENOFIBRATE
Strength Number 160
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