lovastatin - 60505-0179-9 - (lovastatin)

Alphabetical Index


Drug Information of lovastatin

Product NDC: 60505-0179
Proprietary Name: lovastatin
Non Proprietary Name: lovastatin
Active Ingredient(s): 10    mg/1 & nbsp;   lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of lovastatin

Product NDC: 60505-0179
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077748
Marketing Category: ANDA
Start Marketing Date: 20070228

Package Information of lovastatin

Package NDC: 60505-0179-9
Package Description: 90 TABLET in 1 BOTTLE (60505-0179-9)

NDC Information of lovastatin

NDC Code 60505-0179-9
Proprietary Name lovastatin
Package Description 90 TABLET in 1 BOTTLE (60505-0179-9)
Product NDC 60505-0179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070228
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name LOVASTATIN
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of lovastatin


General Information