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Simvastatin - 21695-739-30 - (simvastatin)

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Drug Information of Simvastatin

Product NDC: 21695-739
Proprietary Name: Simvastatin
Non Proprietary Name: simvastatin
Active Ingredient(s): 10    mg/1 & nbsp;   simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Simvastatin

Product NDC: 21695-739
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076685
Marketing Category: ANDA
Start Marketing Date: 20070202

Package Information of Simvastatin

Package NDC: 21695-739-30
Package Description: 30 TABLET in 1 BOTTLE (21695-739-30)

NDC Information of Simvastatin

NDC Code 21695-739-30
Proprietary Name Simvastatin
Package Description 30 TABLET in 1 BOTTLE (21695-739-30)
Product NDC 21695-739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070202
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name SIMVASTATIN
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


General Information