| Product NDC: | 61252-3005 |
| Proprietary Name: | Nicotine UN1654 |
| Non Proprietary Name: | Nicotine UN1654 |
| Active Ingredient(s): | 1 L/L & nbsp; Nicotine UN1654 |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61252-3005 |
| Labeler Name: | Nicobrand LTD |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19970711 |
| Package NDC: | 61252-3005-5 |
| Package Description: | 100 L in 1 DRUM (61252-3005-5) |
| NDC Code | 61252-3005-5 |
| Proprietary Name | Nicotine UN1654 |
| Package Description | 100 L in 1 DRUM (61252-3005-5) |
| Product NDC | 61252-3005 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nicotine UN1654 |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19970711 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nicobrand LTD |
| Substance Name | NICOTINE |
| Strength Number | 1 |
| Strength Unit | L/L |
| Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |