Product NDC: | 37205-344 |
Proprietary Name: | Leader Medicated |
Non Proprietary Name: | TOLNAFTATE |
Active Ingredient(s): | 10 mg/g & nbsp; TOLNAFTATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-344 |
Labeler Name: | Cardinal Health Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080315 |
Package NDC: | 37205-344-66 |
Package Description: | 130 g in 1 CAN (37205-344-66) |
NDC Code | 37205-344-66 |
Proprietary Name | Leader Medicated |
Package Description | 130 g in 1 CAN (37205-344-66) |
Product NDC | 37205-344 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | AEROSOL, POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20080315 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Cardinal Health Inc. |
Substance Name | TOLNAFTATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes |