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simvastatin - 49349-925-38 - (simvastatin)

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Drug Information of simvastatin

Product NDC: 49349-925
Proprietary Name: simvastatin
Non Proprietary Name: simvastatin
Active Ingredient(s): 20    mg/1 & nbsp;   simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of simvastatin

Product NDC: 49349-925
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078155
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of simvastatin

Package NDC: 49349-925-38
Package Description: 3 TABLET, FILM COATED in 1 BLISTER PACK (49349-925-38)

NDC Information of simvastatin

NDC Code 49349-925-38
Proprietary Name simvastatin
Package Description 3 TABLET, FILM COATED in 1 BLISTER PACK (49349-925-38)
Product NDC 49349-925
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130514
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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