VYTORIN - 66582-312-87 - (ezetimibe and simvastatin)

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Drug Information of VYTORIN

Product NDC: 66582-312
Proprietary Name: VYTORIN
Non Proprietary Name: ezetimibe and simvastatin
Active Ingredient(s): 10; 20    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: 66582-312
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021687
Marketing Category: NDA
Start Marketing Date: 20040723

Package Information of VYTORIN

Package NDC: 66582-312-87
Package Description: 10000 TABLET in 1 BOTTLE (66582-312-87)

NDC Information of VYTORIN

NDC Code 66582-312-87
Proprietary Name VYTORIN
Package Description 10000 TABLET in 1 BOTTLE (66582-312-87)
Product NDC 66582-312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ezetimibe and simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040723
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name EZETIMIBE; SIMVASTATIN
Strength Number 10; 20
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