Lovastatin - 0179-1435-90 - (Lovastatin)

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Drug Information of Lovastatin

Product NDC: 0179-1435
Proprietary Name: Lovastatin
Non Proprietary Name: Lovastatin
Active Ingredient(s): 40    mg/1 & nbsp;   Lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lovastatin

Product NDC: 0179-1435
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075636
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Lovastatin

Package NDC: 0179-1435-90
Package Description: 90 TABLET in 1 BOTTLE (0179-1435-90)

NDC Information of Lovastatin

NDC Code 0179-1435-90
Proprietary Name Lovastatin
Package Description 90 TABLET in 1 BOTTLE (0179-1435-90)
Product NDC 0179-1435
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name LOVASTATIN
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lovastatin


General Information