Product NDC: | 56062-029 |
Proprietary Name: | stop smoking aid |
Non Proprietary Name: | Nicotine Polacrilex |
Active Ingredient(s): | 2 mg/1 & nbsp; Nicotine Polacrilex |
Administration Route(s): | ORAL |
Dosage Form(s): | GUM, CHEWING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-029 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076775 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051206 |
Package NDC: | 56062-029-71 |
Package Description: | 5 BLISTER PACK in 1 CARTON (56062-029-71) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Code | 56062-029-71 |
Proprietary Name | stop smoking aid |
Package Description | 5 BLISTER PACK in 1 CARTON (56062-029-71) > 10 GUM, CHEWING in 1 BLISTER PACK |
Product NDC | 56062-029 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Nicotine Polacrilex |
Dosage Form Name | GUM, CHEWING |
Route Name | ORAL |
Start Marketing Date | 20051206 |
Marketing Category Name | ANDA |
Labeler Name | Publix Super Markets Inc |
Substance Name | NICOTINE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes |