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Fenofibrate - 0615-7548-31 - (FENOFIBRATE)

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Drug Information of Fenofibrate

Product NDC: 0615-7548
Proprietary Name: Fenofibrate
Non Proprietary Name: FENOFIBRATE
Active Ingredient(s): 200    mg/1 & nbsp;   FENOFIBRATE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 0615-7548
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075868
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of Fenofibrate

Package NDC: 0615-7548-31
Package Description: 31 CAPSULE in 1 BLISTER PACK (0615-7548-31)

NDC Information of Fenofibrate

NDC Code 0615-7548-31
Proprietary Name Fenofibrate
Package Description 31 CAPSULE in 1 BLISTER PACK (0615-7548-31)
Product NDC 0615-7548
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENOFIBRATE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name FENOFIBRATE
Strength Number 200
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


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