Lovastatin - 68788-9181-6 - (Lovastatin)

Alphabetical Index


Drug Information of Lovastatin

Product NDC: 68788-9181
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: 68788-9181
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075828
Marketing Category: ANDA
Start Marketing Date: 20051027

Package Information of Lovastatin

Package NDC: 68788-9181-6
Package Description: 60 TABLET in 1 BOTTLE, DISPENSING (68788-9181-6)

NDC Information of Lovastatin

NDC Code 68788-9181-6
Proprietary Name Lovastatin
Package Description 60 TABLET in 1 BOTTLE, DISPENSING (68788-9181-6)
Product NDC 68788-9181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lovastatin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051027
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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