Product NDC: | 0363-0124 |
Proprietary Name: | nicotine |
Non Proprietary Name: | Nicotine polacrilex |
Active Ingredient(s): | 2 mg/1 & nbsp; Nicotine polacrilex |
Administration Route(s): | ORAL |
Dosage Form(s): | LOZENGE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0124 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA090711 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090915 |
Package NDC: | 0363-0124-10 |
Package Description: | 4 VIAL in 1 CARTON (0363-0124-10) > 27 LOZENGE in 1 VIAL (0363-0124-09) |
NDC Code | 0363-0124-10 |
Proprietary Name | nicotine |
Package Description | 4 VIAL in 1 CARTON (0363-0124-10) > 27 LOZENGE in 1 VIAL (0363-0124-09) |
Product NDC | 0363-0124 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Nicotine polacrilex |
Dosage Form Name | LOZENGE |
Route Name | ORAL |
Start Marketing Date | 20090915 |
Marketing Category Name | ANDA |
Labeler Name | Walgreen Company |
Substance Name | NICOTINE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes |