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Fenofibrate - 0378-6088-77 - (fenofibrate)

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Drug Information of Fenofibrate

Product NDC: 0378-6088
Proprietary Name: Fenofibrate
Non Proprietary Name: fenofibrate
Active Ingredient(s): 43    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibrate

Product NDC: 0378-6088
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202579
Marketing Category: ANDA
Start Marketing Date: 20130222

Package Information of Fenofibrate

Package NDC: 0378-6088-77
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (0378-6088-77)

NDC Information of Fenofibrate

NDC Code 0378-6088-77
Proprietary Name Fenofibrate
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (0378-6088-77)
Product NDC 0378-6088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130222
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name FENOFIBRATE
Strength Number 43
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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