Simcor - 0074-3312-07 - (Niacin and Simvastatin)

Alphabetical Index


Drug Information of Simcor

Product NDC: 0074-3312
Proprietary Name: Simcor
Non Proprietary Name: Niacin and Simvastatin
Active Ingredient(s): 500; 20    mg/1; mg/1 & nbsp;   Niacin and Simvastatin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Simcor

Product NDC: 0074-3312
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022078
Marketing Category: NDA
Start Marketing Date: 20080215

Package Information of Simcor

Package NDC: 0074-3312-07
Package Description: 1 BOTTLE in 1 CARTON (0074-3312-07) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Simcor

NDC Code 0074-3312-07
Proprietary Name Simcor
Package Description 1 BOTTLE in 1 CARTON (0074-3312-07) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 0074-3312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Niacin and Simvastatin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080215
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name NIACIN; SIMVASTATIN
Strength Number 500; 20
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 Simcor


General Information