Lofibra - 57844-691-98 - (Fenofibrate)

Alphabetical Index


Drug Information of Lofibra

Product NDC: 57844-691
Proprietary Name: Lofibra
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 54    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lofibra

Product NDC: 57844-691
Labeler Name: Teva Select Brands
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076433
Marketing Category: ANDA
Start Marketing Date: 20051123

Package Information of Lofibra

Package NDC: 57844-691-98
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (57844-691-98)

NDC Information of Lofibra

NDC Code 57844-691-98
Proprietary Name Lofibra
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (57844-691-98)
Product NDC 57844-691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051123
Marketing Category Name ANDA
Labeler Name Teva Select Brands
Substance Name FENOFIBRATE
Strength Number 54
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