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: | 61252-3005-4 |
Package Description: | 50 L in 1 DRUM (61252-3005-4) |
NDC Code | 61252-3005-4 |
Proprietary Name | Nicotine UN1654 |
Package Description | 50 L in 1 DRUM (61252-3005-4) |
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] |