| Product NDC: | 0009-5401 |
| Proprietary Name: | Nicotrol |
| Non Proprietary Name: | nicotine |
| Active Ingredient(s): | 10 mg/mL & nbsp; nicotine |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0009-5401 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020385 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960522 |
| Package NDC: | 0009-5401-01 |
| Package Description: | 4 BOTTLE, SPRAY in 1 BOX (0009-5401-01) > 10 mL in 1 BOTTLE, SPRAY |
| NDC Code | 0009-5401-01 |
| Proprietary Name | Nicotrol |
| Package Description | 4 BOTTLE, SPRAY in 1 BOX (0009-5401-01) > 10 mL in 1 BOTTLE, SPRAY |
| Product NDC | 0009-5401 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nicotine |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 19960522 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | NICOTINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |