LOVASTATIN - 54458-914-10 - (LOVASTATIN)

Alphabetical Index


Drug Information of LOVASTATIN

Product NDC: 54458-914
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: 54458-914
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075551
Marketing Category: ANDA
Start Marketing Date: 20080327

Package Information of LOVASTATIN

Package NDC: 54458-914-10
Package Description: 30 TABLET in 1 BLISTER PACK (54458-914-10)

NDC Information of LOVASTATIN

NDC Code 54458-914-10
Proprietary Name LOVASTATIN
Package Description 30 TABLET in 1 BLISTER PACK (54458-914-10)
Product NDC 54458-914
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LOVASTATIN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080327
Marketing Category Name ANDA
Labeler Name International Labs, 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