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Simvastatin - 49349-382-02 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 49349-382
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 20    mg/1 & nbsp;   Simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Simvastatin

Product NDC: 49349-382
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076285
Marketing Category: ANDA
Start Marketing Date: 20110715

Package Information of Simvastatin

Package NDC: 49349-382-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-382-02)

NDC Information of Simvastatin

NDC Code 49349-382-02
Proprietary Name Simvastatin
Package Description 30 TABLET in 1 BLISTER PACK (49349-382-02)
Product NDC 49349-382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110715
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name SIMVASTATIN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


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