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Nicotine Polacrilex
Nicotine Polacrilex - 61252-3004-3 - (Nicotine Polacrilex)
Drug Information of Nicotine Polacrilex
| Product NDC: | 61252-3004 |
| Proprietary Name: | Nicotine Polacrilex |
| Non Proprietary Name: | Nicotine Polacrilex |
| Active Ingredient(s): | 150 g/kg & nbsp; Nicotine Polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicotine Polacrilex
| Product NDC: | 61252-3004 |
| Labeler Name: | Nicobrand LTD |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19940201 |
Package Information of Nicotine Polacrilex
| Package NDC: | 61252-3004-3 |
| Package Description: | 20 kg in 1 DRUM (61252-3004-3) |
NDC Information of Nicotine Polacrilex
| NDC Code | 61252-3004-3 |
| Proprietary Name | Nicotine Polacrilex |
| Package Description | 20 kg in 1 DRUM (61252-3004-3) |
| Product NDC | 61252-3004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 19940201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nicobrand LTD |
| Substance Name | NICOTINE |
| Strength Number | 150 |
| Strength Unit | g/kg |
| Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |
