Lovastatin - 61442-143-10 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 61442-143
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: 61442-143
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075991
Marketing Category: ANDA
Start Marketing Date: 20021125

Package Information of Lovastatin

Package NDC: 61442-143-10
Package Description: 1000 TABLET in 1 BOTTLE (61442-143-10)

NDC Information of Lovastatin

NDC Code 61442-143-10
Proprietary Name Lovastatin
Package Description 1000 TABLET in 1 BOTTLE (61442-143-10)
Product NDC 61442-143
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021125
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, 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