Tricor - 49999-885-30 - (Fenofibrate)

Alphabetical Index


Drug Information of Tricor

Product NDC: 49999-885
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: 49999-885
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021656
Marketing Category: NDA
Start Marketing Date: 20120320

Package Information of Tricor

Package NDC: 49999-885-30
Package Description: 30 TABLET in 1 BOTTLE (49999-885-30)

NDC Information of Tricor

NDC Code 49999-885-30
Proprietary Name Tricor
Package Description 30 TABLET in 1 BOTTLE (49999-885-30)
Product NDC 49999-885
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenofibrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120320
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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