Product NDC: | 51672-2020 |
Proprietary Name: | Tolnaftate Antifungal |
Non Proprietary Name: | Tolnaftate |
Active Ingredient(s): | 1 g/100g & nbsp; Tolnaftate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-2020 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19950101 |
Package NDC: | 51672-2020-1 |
Package Description: | 1 TUBE in 1 CARTON (51672-2020-1) > 15 g in 1 TUBE |
NDC Code | 51672-2020-1 |
Proprietary Name | Tolnaftate Antifungal |
Package Description | 1 TUBE in 1 CARTON (51672-2020-1) > 15 g in 1 TUBE |
Product NDC | 51672-2020 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tolnaftate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19950101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | TOLNAFTATE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |