Simcor - 54868-5886-0 - (simvastatin and niacin)

Alphabetical Index


Drug Information of Simcor

Product NDC: 54868-5886
Proprietary Name: Simcor
Non Proprietary Name: simvastatin and niacin
Active Ingredient(s): 500; 20    mg/1; mg/1 & nbsp;   simvastatin and niacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Simcor

Product NDC: 54868-5886
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022078
Marketing Category: NDA
Start Marketing Date: 20080505

Package Information of Simcor

Package NDC: 54868-5886-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5886-0)

NDC Information of Simcor

NDC Code 54868-5886-0
Proprietary Name Simcor
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5886-0)
Product NDC 54868-5886
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name simvastatin and niacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080505
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name NIACIN; SIMVASTATIN
Strength Number 500; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA],Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient]

Complete Information of Simcor


General Information