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Simvastatin - 55154-4782-0 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 55154-4782
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: 55154-4782
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078103
Marketing Category: ANDA
Start Marketing Date: 20110502

Package Information of Simvastatin

Package NDC: 55154-4782-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4782-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Simvastatin

NDC Code 55154-4782-0
Proprietary Name Simvastatin
Package Description 10 BLISTER PACK in 1 BAG (55154-4782-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-4782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110502
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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