Niaspan - 54868-0017-6 - (Niacin)

Alphabetical Index


Drug Information of Niaspan

Product NDC: 54868-0017
Proprietary Name: Niaspan
Non Proprietary Name: Niacin
Active Ingredient(s): 1000    mg/1 & nbsp;   Niacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Niaspan

Product NDC: 54868-0017
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020381
Marketing Category: NDA
Start Marketing Date: 20090512

Package Information of Niaspan

Package NDC: 54868-0017-6
Package Description: 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-0017-6)

NDC Information of Niaspan

NDC Code 54868-0017-6
Proprietary Name Niaspan
Package Description 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-0017-6)
Product NDC 54868-0017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Niacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090512
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name NIACIN
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient]

Complete Information of Niaspan


General Information