| Product NDC: | 0536-3030 |
| Proprietary Name: | Rugby Nicotine Polacrilex Gum, Original 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: | 0536-3030 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074707 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990319 |
| Package NDC: | 0536-3030-06 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0536-3030-06) > 10 GUM, CHEWING in 1 BLISTER PACK |
| NDC Code | 0536-3030-06 |
| Proprietary Name | Rugby Nicotine Polacrilex Gum, Original Flavor |
| Package Description | 5 BLISTER PACK in 1 CARTON (0536-3030-06) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 0536-3030 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | BUCCAL |
| Start Marketing Date | 19990319 |
| Marketing Category Name | ANDA |
| Labeler Name | Rugby Laboratories |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |