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Simvastatin - 0093-7154-93 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 0093-7154
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: 0093-7154
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076052
Marketing Category: ANDA
Start Marketing Date: 20060627

Package Information of Simvastatin

Package NDC: 0093-7154-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-7154-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7154-19)

NDC Information of Simvastatin

NDC Code 0093-7154-93
Proprietary Name Simvastatin
Package Description 100 BLISTER PACK in 1 BOX (0093-7154-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7154-19)
Product NDC 0093-7154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060627
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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