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Simvastatin - 63739-572-10 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 63739-572
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: 63739-572
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077691
Marketing Category: ANDA
Start Marketing Date: 20121122

Package Information of Simvastatin

Package NDC: 63739-572-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-572-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Simvastatin

NDC Code 63739-572-10
Proprietary Name Simvastatin
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-572-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-572
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121122
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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