Lovastatin - 42291-376-90 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 42291-376
Proprietary Name: Lovastatin
Non Proprietary Name: Lovastatin
Active Ingredient(s): 20    mg/1 & nbsp;   Lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lovastatin

Product NDC: 42291-376
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075991
Marketing Category: ANDA
Start Marketing Date: 20020606

Package Information of Lovastatin

Package NDC: 42291-376-90
Package Description: 90 TABLET in 1 BOTTLE (42291-376-90)

NDC Information of Lovastatin

NDC Code 42291-376-90
Proprietary Name Lovastatin
Package Description 90 TABLET in 1 BOTTLE (42291-376-90)
Product NDC 42291-376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020606
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name LOVASTATIN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Lovastatin


General Information