Product NDC: | 49035-196 |
Proprietary Name: | NICOTINE |
Non Proprietary Name: | nicotine |
Active Ingredient(s): | 7 mg/24h & nbsp; nicotine |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-196 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020165 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20101019 |
Package NDC: | 49035-196-02 |
Package Description: | 14 PATCH in 1 CARTON (49035-196-02) > 24 h in 1 PATCH |
NDC Code | 49035-196-02 |
Proprietary Name | NICOTINE |
Package Description | 14 PATCH in 1 CARTON (49035-196-02) > 24 h in 1 PATCH |
Product NDC | 49035-196 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | nicotine |
Dosage Form Name | PATCH, EXTENDED RELEASE |
Route Name | TRANSDERMAL |
Start Marketing Date | 20101019 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Wal-Mart Stores Inc |
Substance Name | NICOTINE |
Strength Number | 7 |
Strength Unit | mg/24h |
Pharmaceutical Classes |