Product NDC: | 61252-3006 |
Proprietary Name: | nicotine tartrate |
Non Proprietary Name: | nicotine tartrate |
Active Ingredient(s): | 1 kg/kg & nbsp; nicotine tartrate |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61252-3006 |
Labeler Name: | Nicobrand LTD |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19970711 |
Package NDC: | 61252-3006-8 |
Package Description: | 25 kg in 1 BOX (61252-3006-8) |
NDC Code | 61252-3006-8 |
Proprietary Name | nicotine tartrate |
Package Description | 25 kg in 1 BOX (61252-3006-8) |
Product NDC | 61252-3006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nicotine tartrate |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 19970711 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Nicobrand LTD |
Substance Name | NICOTINE BITARTRATE ANHYDROUS |
Strength Number | 1 |
Strength Unit | kg/kg |
Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |