Tricor - 0074-6122-71 - (Fenofibrate)

Alphabetical Index


Drug Information of Tricor

Product NDC: 0074-6122
Proprietary Name: Tricor
Non Proprietary Name: Fenofibrate
Active Ingredient(s): 48    mg/1 & nbsp;   Fenofibrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tricor

Product NDC: 0074-6122
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021656
Marketing Category: NDA
Start Marketing Date: 20041105

Package Information of Tricor

Package NDC: 0074-6122-71
Package Description: 4 BLISTER PACK in 1 CARTON (0074-6122-71) > 7 TABLET in 1 BLISTER PACK

NDC Information of Tricor

NDC Code 0074-6122-71
Proprietary Name Tricor
Package Description 4 BLISTER PACK in 1 CARTON (0074-6122-71) > 7 TABLET in 1 BLISTER PACK
Product NDC 0074-6122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041105
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name FENOFIBRATE
Strength Number 48
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