Advicor - 0074-3005-90 - (niacin and lovastatin)

Alphabetical Index


Drug Information of Advicor

Product NDC: 0074-3005
Proprietary Name: Advicor
Non Proprietary Name: niacin and lovastatin
Active Ingredient(s): 20; 500    mg/1; mg/1 & nbsp;   niacin and lovastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Advicor

Product NDC: 0074-3005
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021249
Marketing Category: NDA
Start Marketing Date: 20011217

Package Information of Advicor

Package NDC: 0074-3005-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3005-90)

NDC Information of Advicor

NDC Code 0074-3005-90
Proprietary Name Advicor
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3005-90)
Product NDC 0074-3005
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name niacin and lovastatin
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20011217
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name LOVASTATIN; NIACIN
Strength Number 20; 500
Strength Unit mg/1; mg/1
Pharmaceutical Classes Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Advicor


General Information