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Fenofibric Acid - 53489-678-90 - (Fenofibric Acid)

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Drug Information of Fenofibric Acid

Product NDC: 53489-678
Proprietary Name: Fenofibric Acid
Non Proprietary Name: Fenofibric Acid
Active Ingredient(s): 105    mg/1 & nbsp;   Fenofibric Acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fenofibric Acid

Product NDC: 53489-678
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022418
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20090831

Package Information of Fenofibric Acid

Package NDC: 53489-678-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (53489-678-90)

NDC Information of Fenofibric Acid

NDC Code 53489-678-90
Proprietary Name Fenofibric Acid
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (53489-678-90)
Product NDC 53489-678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibric Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090831
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name FENOFIBRIC ACID
Strength Number 105
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC]

Complete Information of Fenofibric Acid


General Information