CHANTIX - 0069-0469-97 - (varenicline tartrate)

Alphabetical Index


Drug Information of CHANTIX

Product NDC: 0069-0469
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: 0069-0469
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021928
Marketing Category: NDA
Start Marketing Date: 20060510

Package Information of CHANTIX

Package NDC: 0069-0469-97
Package Description: 4 BLISTER PACK in 1 CARTON (0069-0469-97) > 14 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of CHANTIX

NDC Code 0069-0469-97
Proprietary Name CHANTIX
Package Description 4 BLISTER PACK in 1 CARTON (0069-0469-97) > 14 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0069-0469
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 Pfizer Laboratories Div Pfizer Inc
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