Lovastatin - 52125-405-20 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 52125-405
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: 52125-405
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075991
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of Lovastatin

Package NDC: 52125-405-20
Package Description: 100 TABLET in 1 VIAL (52125-405-20)

NDC Information of Lovastatin

NDC Code 52125-405-20
Proprietary Name Lovastatin
Package Description 100 TABLET in 1 VIAL (52125-405-20)
Product NDC 52125-405
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130514
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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