lovastatin - 53489-609-07 - (lovastatin)

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Drug Information of lovastatin

Product NDC: 53489-609
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: 53489-609
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077520
Marketing Category: ANDA
Start Marketing Date: 20060414

Package Information of lovastatin

Package NDC: 53489-609-07
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (53489-609-07)

NDC Information of lovastatin

NDC Code 53489-609-07
Proprietary Name lovastatin
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (53489-609-07)
Product NDC 53489-609
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060414
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
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