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Simvastatin - 42571-020-60 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 42571-020
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 20    mg/1 & nbsp;   Simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Simvastatin

Product NDC: 42571-020
Labeler Name: Micro Labs Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090383
Marketing Category: ANDA
Start Marketing Date: 20121109

Package Information of Simvastatin

Package NDC: 42571-020-60
Package Description: 60 TABLET in 1 BOTTLE (42571-020-60)

NDC Information of Simvastatin

NDC Code 42571-020-60
Proprietary Name Simvastatin
Package Description 60 TABLET in 1 BOTTLE (42571-020-60)
Product NDC 42571-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121109
Marketing Category Name ANDA
Labeler Name Micro Labs Limited
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