| Product NDC: | 0536-3113 |
| Proprietary Name: | Rugby Nicotine Polacrilex Gum, Coated Mint Flavor |
| Non Proprietary Name: | Nicotine Polacrilex |
| Active Ingredient(s): | 4 mg/1 & nbsp; Nicotine Polacrilex |
| Administration Route(s): | BUCCAL |
| Dosage Form(s): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0536-3113 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078697 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081229 |
| Package NDC: | 0536-3113-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0536-3113-01) > 10 GUM, CHEWING in 1 BLISTER PACK |
| NDC Code | 0536-3113-01 |
| Proprietary Name | Rugby Nicotine Polacrilex Gum, Coated Mint Flavor |
| Package Description | 10 BLISTER PACK in 1 CARTON (0536-3113-01) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 0536-3113 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | BUCCAL |
| Start Marketing Date | 20081229 |
| Marketing Category Name | ANDA |
| Labeler Name | Rugby Laboratories |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |