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CHANTIX
CHANTIX - 0069-0469-12 - (varenicline tartrate)
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: | 0069-0469-12 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0069-0469-12) > 28 TABLET, FILM COATED in 1 BLISTER PACK (0069-0469-11) |
NDC Information of CHANTIX
| NDC Code | 0069-0469-12 |
| Proprietary Name | CHANTIX |
| Package Description | 2 BLISTER PACK in 1 CARTON (0069-0469-12) > 28 TABLET, FILM COATED in 1 BLISTER PACK (0069-0469-11) |
| 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] |
