Niaspan - 35356-301-90 - (Niacin)

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Drug Information of Niaspan

Product NDC: 35356-301
Proprietary Name: Niaspan
Non Proprietary Name: Niacin
Active Ingredient(s): 750    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: 35356-301
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020381
Marketing Category: NDA
Start Marketing Date: 20120403

Package Information of Niaspan

Package NDC: 35356-301-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (35356-301-90)

NDC Information of Niaspan

NDC Code 35356-301-90
Proprietary Name Niaspan
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (35356-301-90)
Product NDC 35356-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Niacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120403
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name NIACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient]

Complete Information of Niaspan


General Information