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simvastatin - 68788-9869-3 - (simvastatin)

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Drug Information of simvastatin

Product NDC: 68788-9869
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: 68788-9869
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078155
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of simvastatin

Package NDC: 68788-9869-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9869-3)

NDC Information of simvastatin

NDC Code 68788-9869-3
Proprietary Name simvastatin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68788-9869-3)
Product NDC 68788-9869
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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


General Information