Product NDC: | 41268-532 |
Proprietary Name: | nicotine |
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: | 41268-532 |
Labeler Name: | Hannaford Brothers Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076779 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090216 |
Package NDC: | 41268-532-78 |
Package Description: | 10 BLISTER PACK in 1 CARTON (41268-532-78) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Code | 41268-532-78 |
Proprietary Name | nicotine |
Package Description | 10 BLISTER PACK in 1 CARTON (41268-532-78) > 10 GUM, CHEWING in 1 BLISTER PACK |
Product NDC | 41268-532 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Nicotine Polacrilex |
Dosage Form Name | GUM, CHEWING |
Route Name | ORAL |
Start Marketing Date | 20090216 |
Marketing Category Name | ANDA |
Labeler Name | Hannaford Brothers Company |
Substance Name | NICOTINE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes |