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NICODERM
NICODERM - 0135-0194-01 - (nicotine)
Drug Information of NICODERM
| Product NDC: | 0135-0194 |
| Proprietary Name: | NICODERM |
| Non Proprietary Name: | nicotine |
| Active Ingredient(s): | 21 mg/24h & nbsp; nicotine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NICODERM
| Product NDC: | 0135-0194 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020165 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110512 |
Package Information of NICODERM
| Package NDC: | 0135-0194-01 |
| Package Description: | 7 PATCH in 1 CARTON (0135-0194-01) > 24 h in 1 PATCH |
NDC Information of NICODERM
| NDC Code | 0135-0194-01 |
| Proprietary Name | NICODERM |
| Package Description | 7 PATCH in 1 CARTON (0135-0194-01) > 24 h in 1 PATCH |
| Product NDC | 0135-0194 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | nicotine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20110512 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | NICOTINE |
| Strength Number | 21 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes |
