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 |