Chantix - 21695-946-56 - (varenicline tartrate)

Alphabetical Index


Drug Information of Chantix

Product NDC: 21695-946
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: 21695-946
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021928
Marketing Category: NDA
Start Marketing Date: 20060510

Package Information of Chantix

Package NDC: 21695-946-56
Package Description: 56 TABLET, FILM COATED in 1 BOTTLE (21695-946-56)

NDC Information of Chantix

NDC Code 21695-946-56
Proprietary Name Chantix
Package Description 56 TABLET, FILM COATED in 1 BOTTLE (21695-946-56)
Product NDC 21695-946
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name varenicline tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060510
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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