Product NDC: | 63539-5195 |
Proprietary Name: | Nicotrol (Professional Sample) |
Non Proprietary Name: | nicotine |
Active Ingredient(s): | 4 mg/1 & nbsp; nicotine |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | INHALANT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63539-5195 |
Labeler Name: | U.S. Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020714 |
Marketing Category: | NDA |
Start Marketing Date: | 19970502 |
Package NDC: | 63539-5195-1 |
Package Description: | 7 TRAY in 1 CARTON (63539-5195-1) > 1 CARTRIDGE in 1 TRAY > 6 INHALANT in 1 CARTRIDGE |
NDC Code | 63539-5195-1 |
Proprietary Name | Nicotrol (Professional Sample) |
Package Description | 7 TRAY in 1 CARTON (63539-5195-1) > 1 CARTRIDGE in 1 TRAY > 6 INHALANT in 1 CARTRIDGE |
Product NDC | 63539-5195 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nicotine |
Dosage Form Name | INHALANT |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19970502 |
Marketing Category Name | NDA |
Labeler Name | U.S. Pharmaceuticals |
Substance Name | NICOTINE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |