Lofibra - 57844-322-01 - (Fenofibrate)

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Drug Information of Lofibra

Product NDC: 57844-322
Proprietary Name: Lofibra
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 67    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Lofibra

Product NDC: 57844-322
Labeler Name: Teva Select Brands
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075753
Marketing Category: ANDA
Start Marketing Date: 20021011

Package Information of Lofibra

Package NDC: 57844-322-01
Package Description: 100 CAPSULE in 1 BOTTLE (57844-322-01)

NDC Information of Lofibra

NDC Code 57844-322-01
Proprietary Name Lofibra
Package Description 100 CAPSULE in 1 BOTTLE (57844-322-01)
Product NDC 57844-322
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20021011
Marketing Category Name ANDA
Labeler Name Teva Select Brands
Substance Name FENOFIBRATE
Strength Number 67
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 Lofibra


General Information