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Simvastatin - 55154-5378-0 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 55154-5378
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 10    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: 55154-5378
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090868
Marketing Category: ANDA
Start Marketing Date: 20111003

Package Information of Simvastatin

Package NDC: 55154-5378-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5378-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Simvastatin

NDC Code 55154-5378-0
Proprietary Name Simvastatin
Package Description 10 BLISTER PACK in 1 BAG (55154-5378-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111003
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name SIMVASTATIN
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


General Information