VYTORIN - 54868-5259-1 - (ezetimibe and simvastatin)

Alphabetical Index


Drug Information of VYTORIN

Product NDC: 54868-5259
Proprietary Name: VYTORIN
Non Proprietary Name: ezetimibe and simvastatin
Active Ingredient(s): 10; 80    mg/1; mg/1 & nbsp;   ezetimibe and simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of VYTORIN

Product NDC: 54868-5259
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021687
Marketing Category: NDA
Start Marketing Date: 20050404

Package Information of VYTORIN

Package NDC: 54868-5259-1
Package Description: 90 TABLET in 1 BOTTLE (54868-5259-1)

NDC Information of VYTORIN

NDC Code 54868-5259-1
Proprietary Name VYTORIN
Package Description 90 TABLET in 1 BOTTLE (54868-5259-1)
Product NDC 54868-5259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ezetimibe and simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050404
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name EZETIMIBE; SIMVASTATIN
Strength Number 10; 80
Strength Unit mg/1; mg/1
Pharmaceutical Classes Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of VYTORIN


General Information