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Simvastatin - 68645-262-54 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 68645-262
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 40    mg/1 & nbsp;   Simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Simvastatin

Product NDC: 68645-262
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077752
Marketing Category: ANDA
Start Marketing Date: 20101001

Package Information of Simvastatin

Package NDC: 68645-262-54
Package Description: 30 TABLET in 1 BOTTLE (68645-262-54)

NDC Information of Simvastatin

NDC Code 68645-262-54
Proprietary Name Simvastatin
Package Description 30 TABLET in 1 BOTTLE (68645-262-54)
Product NDC 68645-262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101001
Marketing Category Name ANDA
Labeler Name Legacy Pharmaceutical Packaging
Substance Name SIMVASTATIN
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


General Information