ZOCOR - 49999-306-30 - (simvastatin)

Alphabetical Index


Drug Information of ZOCOR

Product NDC: 49999-306
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: 49999-306
Labeler Name: Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019766
Marketing Category: NDA
Start Marketing Date: 20110808

Package Information of ZOCOR

Package NDC: 49999-306-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-306-30)

NDC Information of ZOCOR

NDC Code 49999-306-30
Proprietary Name ZOCOR
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-306-30)
Product NDC 49999-306
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110808
Marketing Category Name NDA
Labeler Name Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC
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