Chantix - 35356-012-56 - (varenicline tartrate)

Alphabetical Index


Drug Information of Chantix

Product NDC: 35356-012
Proprietary Name: Chantix
Non Proprietary Name: varenicline tartrate
Active Ingredient(s): 1    mg/1 & nbsp;   varenicline tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Chantix

Product NDC: 35356-012
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021928
Marketing Category: NDA
Start Marketing Date: 20120223

Package Information of Chantix

Package NDC: 35356-012-56
Package Description: 56 TABLET, FILM COATED in 1 BOTTLE (35356-012-56)

NDC Information of Chantix

NDC Code 35356-012-56
Proprietary Name Chantix
Package Description 56 TABLET, FILM COATED in 1 BOTTLE (35356-012-56)
Product NDC 35356-012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name varenicline tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120223
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name VARENICLINE TARTRATE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Partial Cholinergic Nicotinic Agonist [EPC],Partial Cholinergic Nicotinic Agonists [MoA]

Complete Information of Chantix


General Information