Niaspan - 68258-6037-6 - (Niacin)

Alphabetical Index


Drug Information of Niaspan

Product NDC: 68258-6037
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: 68258-6037
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020381
Marketing Category: NDA
Start Marketing Date: 19970728

Package Information of Niaspan

Package NDC: 68258-6037-6
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68258-6037-6)

NDC Information of Niaspan

NDC Code 68258-6037-6
Proprietary Name Niaspan
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68258-6037-6)
Product NDC 68258-6037
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Niacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19970728
Marketing Category Name NDA
Labeler Name Dispensing Solutions, 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