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Simvastatin - 68180-482-09 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 68180-482
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 5    mg/1 & nbsp;   Simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Simvastatin

Product NDC: 68180-482
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078103
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Simvastatin

Package NDC: 68180-482-09
Package Description: 90 TABLET in 1 BOTTLE (68180-482-09)

NDC Information of Simvastatin

NDC Code 68180-482-09
Proprietary Name Simvastatin
Package Description 90 TABLET in 1 BOTTLE (68180-482-09)
Product NDC 68180-482
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name SIMVASTATIN
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


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