Altoprev - 59630-630-30 - (lovastatin)

Alphabetical Index


Drug Information of Altoprev

Product NDC: 59630-630
Proprietary Name: Altoprev
Non Proprietary Name: lovastatin
Active Ingredient(s): 60    mg/1 & nbsp;   lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Altoprev

Product NDC: 59630-630
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021316
Marketing Category: NDA
Start Marketing Date: 20020626

Package Information of Altoprev

Package NDC: 59630-630-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59630-630-30)

NDC Information of Altoprev

NDC Code 59630-630-30
Proprietary Name Altoprev
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59630-630-30)
Product NDC 59630-630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lovastatin
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020626
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name LOVASTATIN
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Altoprev


General Information