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NICOTINE TRANSDERMAL SYSTEM
NICOTINE TRANSDERMAL SYSTEM - 0067-5126-09 - (NICOTINE)
Drug Information of NICOTINE TRANSDERMAL SYSTEM
| Product NDC: | 0067-5126 |
| Proprietary Name: | NICOTINE TRANSDERMAL SYSTEM |
| Non Proprietary Name: | NICOTINE |
| Active Ingredient(s): | 21 mg/24h & nbsp; NICOTINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NICOTINE TRANSDERMAL SYSTEM
| Product NDC: | 0067-5126 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020076 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19991112 |
Package Information of NICOTINE TRANSDERMAL SYSTEM
| Package NDC: | 0067-5126-09 |
| Package Description: | 1 PATCH in 1 POUCH (0067-5126-09) > 24 h in 1 PATCH |
NDC Information of NICOTINE TRANSDERMAL SYSTEM
| NDC Code | 0067-5126-09 |
| Proprietary Name | NICOTINE TRANSDERMAL SYSTEM |
| Package Description | 1 PATCH in 1 POUCH (0067-5126-09) > 24 h in 1 PATCH |
| Product NDC | 0067-5126 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NICOTINE |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TOPICAL |
| Start Marketing Date | 19991112 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | NICOTINE |
| Strength Number | 21 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes |
