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NICOTINE
NICOTINE - 0363-0209-01 - (nicotine polacrilex)
Drug Information of NICOTINE
| Product NDC: | 0363-0209 |
| Proprietary Name: | NICOTINE |
| Non Proprietary Name: | nicotine polacrilex |
| Active Ingredient(s): | 4 mg/1 & nbsp; nicotine polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NICOTINE
| Product NDC: | 0363-0209 |
| Labeler Name: | Walgreens |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021330 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20021031 |
Package Information of NICOTINE
| Package NDC: | 0363-0209-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0363-0209-01) > 72 LOZENGE in 1 BLISTER PACK |
NDC Information of NICOTINE
| NDC Code | 0363-0209-01 |
| Proprietary Name | NICOTINE |
| Package Description | 1 BLISTER PACK in 1 CARTON (0363-0209-01) > 72 LOZENGE in 1 BLISTER PACK |
| Product NDC | 0363-0209 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | nicotine polacrilex |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20021031 |
| Marketing Category Name | NDA |
| Labeler Name | Walgreens |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
