Product NDC: | 0069-0471 |
Proprietary Name: | CHANTIX |
Non Proprietary Name: | varenicline tartrate |
Active Ingredient(s): | & nbsp; varenicline tartrate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0471 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021928 |
Marketing Category: | NDA |
Start Marketing Date: | 20060510 |
Package NDC: | 0069-0471-97 |
Package Description: | 1 KIT in 1 CARTON (0069-0471-97) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 0069-0471-97 |
Proprietary Name | CHANTIX |
Package Description | 1 KIT in 1 CARTON (0069-0471-97) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 0069-0471 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | varenicline tartrate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20060510 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |