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Simvastatin - 63304-789-10 - (simvastatin)

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Drug Information of Simvastatin

Product NDC: 63304-789
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: 63304-789
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076285
Marketing Category: ANDA
Start Marketing Date: 20061220

Package Information of Simvastatin

Package NDC: 63304-789-10
Package Description: 1000 TABLET in 1 BOTTLE (63304-789-10)

NDC Information of Simvastatin

NDC Code 63304-789-10
Proprietary Name Simvastatin
Package Description 1000 TABLET in 1 BOTTLE (63304-789-10)
Product NDC 63304-789
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061220
Marketing Category Name ANDA
Labeler Name Ranbaxy 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


General Information