| Product NDC: | 59779-170 | 
| Proprietary Name: | nicotine polacrilex | 
| Non Proprietary Name: | Nicotine Polacrilex | 
| Active Ingredient(s): | 4 mg/1 & nbsp; Nicotine Polacrilex | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | GUM, CHEWING | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-170 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA076789 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20050707 | 
| Package NDC: | 59779-170-25 | 
| Package Description: | 11 BLISTER PACK in 1 CARTON (59779-170-25) > 10 GUM, CHEWING in 1 BLISTER PACK | 
| NDC Code | 59779-170-25 | 
| Proprietary Name | nicotine polacrilex | 
| Package Description | 11 BLISTER PACK in 1 CARTON (59779-170-25) > 10 GUM, CHEWING in 1 BLISTER PACK | 
| Product NDC | 59779-170 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Nicotine Polacrilex | 
| Dosage Form Name | GUM, CHEWING | 
| Route Name | ORAL | 
| Start Marketing Date | 20050707 | 
| Marketing Category Name | ANDA | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | NICOTINE | 
| Strength Number | 4 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |