| Product NDC: | 0067-6045 |
| Proprietary Name: | NICOTINE TRANSDERMAL SYSTEM |
| Non Proprietary Name: | NICOTINE |
| Active Ingredient(s): | & nbsp; NICOTINE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0067-6045 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020076 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040721 |
| Package NDC: | 0067-6045-56 |
| Package Description: | 1 KIT in 1 CARTON (0067-6045-56) * 28 PATCH in 1 CONTAINER (0067-5126-09) > 24 h in 1 PATCH * 14 PATCH in 1 CARTON (0067-5125-09) > 24 h in 1 PATCH * 14 PATCH in 1 CARTON (0067-5124-09) > 24 h in 1 PATCH |
| NDC Code | 0067-6045-56 |
| Proprietary Name | NICOTINE TRANSDERMAL SYSTEM |
| Package Description | 1 KIT in 1 CARTON (0067-6045-56) * 28 PATCH in 1 CONTAINER (0067-5126-09) > 24 h in 1 PATCH * 14 PATCH in 1 CARTON (0067-5125-09) > 24 h in 1 PATCH * 14 PATCH in 1 CARTON (0067-5124-09) > 24 h in 1 PATCH |
| Product NDC | 0067-6045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NICOTINE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20040721 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |