Product NDC: | 0536-3029 |
Proprietary Name: | Rugby Nicotine Polacrilex Gum, Original Flavor |
Non Proprietary Name: | Nicotine Polacrilex |
Active Ingredient(s): | 2 mg/1 & nbsp; Nicotine Polacrilex |
Administration Route(s): | BUCCAL |
Dosage Form(s): | GUM, CHEWING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0536-3029 |
Labeler Name: | Rugby Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074507 |
Marketing Category: | ANDA |
Start Marketing Date: | 19990315 |
Package NDC: | 0536-3029-23 |
Package Description: | 11 BLISTER PACK in 1 CARTON (0536-3029-23) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Code | 0536-3029-23 |
Proprietary Name | Rugby Nicotine Polacrilex Gum, Original Flavor |
Package Description | 11 BLISTER PACK in 1 CARTON (0536-3029-23) > 10 GUM, CHEWING in 1 BLISTER PACK |
Product NDC | 0536-3029 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Nicotine Polacrilex |
Dosage Form Name | GUM, CHEWING |
Route Name | BUCCAL |
Start Marketing Date | 19990315 |
Marketing Category Name | ANDA |
Labeler Name | Rugby Laboratories |
Substance Name | NICOTINE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes |