| Product NDC: | 11673-190 |
| 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): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-190 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090711 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110312 |
| Package NDC: | 11673-190-06 |
| Package Description: | 4 VIAL in 1 CARTON (11673-190-06) > 24 LOZENGE in 1 VIAL |
| NDC Code | 11673-190-06 |
| Proprietary Name | nicotine polacrilex |
| Package Description | 4 VIAL in 1 CARTON (11673-190-06) > 24 LOZENGE in 1 VIAL |
| Product NDC | 11673-190 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20110312 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |