ZOCOR - 0006-0740-54 - (SIMVASTATIN)

Alphabetical Index


Drug Information of ZOCOR

Product NDC: 0006-0740
Proprietary Name: ZOCOR
Non Proprietary Name: SIMVASTATIN
Active Ingredient(s): 20    mg/1 & nbsp;   SIMVASTATIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZOCOR

Product NDC: 0006-0740
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019766
Marketing Category: NDA
Start Marketing Date: 19911223

Package Information of ZOCOR

Package NDC: 0006-0740-54
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0006-0740-54)

NDC Information of ZOCOR

NDC Code 0006-0740-54
Proprietary Name ZOCOR
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0006-0740-54)
Product NDC 0006-0740
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SIMVASTATIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19911223
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name SIMVASTATIN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of ZOCOR


General Information