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Simvastatin - 49349-356-02 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 49349-356
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: 49349-356
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077691
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Simvastatin

Package NDC: 49349-356-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-356-02)

NDC Information of Simvastatin

NDC Code 49349-356-02
Proprietary Name Simvastatin
Package Description 30 TABLET in 1 BLISTER PACK (49349-356-02)
Product NDC 49349-356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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


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