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NICORETTE
NICORETTE - 0135-0514-03 - (nicotine polacrilex)
Drug Information of NICORETTE
| Product NDC: | 0135-0514 |
| Proprietary Name: | NICORETTE |
| Non Proprietary Name: | nicotine polacrilex |
| Active Ingredient(s): | 2 mg/1 & nbsp; nicotine polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NICORETTE
| Product NDC: | 0135-0514 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021330 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101019 |
Package Information of NICORETTE
| Package NDC: | 0135-0514-03 |
| Package Description: | 108 LOZENGE in 1 CONTAINER (0135-0514-03) |
NDC Information of NICORETTE
| NDC Code | 0135-0514-03 |
| Proprietary Name | NICORETTE |
| Package Description | 108 LOZENGE in 1 CONTAINER (0135-0514-03) |
| Product NDC | 0135-0514 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | nicotine polacrilex |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
