Home > National Drug Code (NDC) > Simvastatin

Simvastatin - 0615-7706-39 - (Simvastatin)

Alphabetical Index


Drug Information of Simvastatin

Product NDC: 0615-7706
Proprietary Name: Simvastatin
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 Simvastatin

Product NDC: 0615-7706
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077691
Marketing Category: ANDA
Start Marketing Date: 20061220

Package Information of Simvastatin

Package NDC: 0615-7706-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7706-39)

NDC Information of Simvastatin

NDC Code 0615-7706-39
Proprietary Name Simvastatin
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7706-39)
Product NDC 0615-7706
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061220
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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 Simvastatin


General Information