Niaspan - 21695-852-90 - (Niacin)

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Drug Information of Niaspan

Product NDC: 21695-852
Proprietary Name: Niaspan
Non Proprietary Name: Niacin
Active Ingredient(s): 500    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: 21695-852
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020381
Marketing Category: NDA
Start Marketing Date: 20100310

Package Information of Niaspan

Package NDC: 21695-852-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-852-90)

NDC Information of Niaspan

NDC Code 21695-852-90
Proprietary Name Niaspan
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-852-90)
Product NDC 21695-852
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Niacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100310
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name NIACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient]

Complete Information of Niaspan


General Information