TRICOR - 54569-5750-0 - (fenofibrate)

Alphabetical Index


Drug Information of TRICOR

Product NDC: 54569-5750
Proprietary Name: TRICOR
Non Proprietary Name: fenofibrate
Active Ingredient(s): 145    mg/1 & nbsp;   fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TRICOR

Product NDC: 54569-5750
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021656
Marketing Category: NDA
Start Marketing Date: 20051107

Package Information of TRICOR

Package NDC: 54569-5750-0
Package Description: 30 TABLET in 1 BOTTLE (54569-5750-0)

NDC Information of TRICOR

NDC Code 54569-5750-0
Proprietary Name TRICOR
Package Description 30 TABLET in 1 BOTTLE (54569-5750-0)
Product NDC 54569-5750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051107
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
Substance Name FENOFIBRATE
Strength Number 145
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 TRICOR


General Information