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Simvastatin - 24658-302-10 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 24658-302
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: 24658-302
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078034
Marketing Category: ANDA
Start Marketing Date: 20111017

Package Information of Simvastatin

Package NDC: 24658-302-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (24658-302-10)

NDC Information of Simvastatin

NDC Code 24658-302-10
Proprietary Name Simvastatin
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (24658-302-10)
Product NDC 24658-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111017
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, 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 Simvastatin


General Information