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Simvastatin - 67046-675-30 - (Simvastatin)

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Drug Information of Simvastatin

Product NDC: 67046-675
Proprietary Name: Simvastatin
Non Proprietary Name: Simvastatin
Active Ingredient(s): 5    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: 67046-675
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077837
Marketing Category: ANDA
Start Marketing Date: 20100825

Package Information of Simvastatin

Package NDC: 67046-675-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-675-30)

NDC Information of Simvastatin

NDC Code 67046-675-30
Proprietary Name Simvastatin
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-675-30)
Product NDC 67046-675
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Simvastatin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100825
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name SIMVASTATIN
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Simvastatin


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