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DermaTAF Antifungal Treatment
DermaTAF Antifungal Treatment - 50080-002-15 - (TOLNAFTATE)
Drug Information of DermaTAF Antifungal Treatment
| Product NDC: | 50080-002 |
| Proprietary Name: | DermaTAF Antifungal Treatment |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DermaTAF Antifungal Treatment
| Product NDC: | 50080-002 |
| Labeler Name: | DermaTAF, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130115 |
Package Information of DermaTAF Antifungal Treatment
| Package NDC: | 50080-002-15 |
| Package Description: | 1 BOTTLE in 1 BOX (50080-002-15) > 15 mL in 1 BOTTLE |
NDC Information of DermaTAF Antifungal Treatment
| NDC Code | 50080-002-15 |
| Proprietary Name | DermaTAF Antifungal Treatment |
| Package Description | 1 BOTTLE in 1 BOX (50080-002-15) > 15 mL in 1 BOTTLE |
| Product NDC | 50080-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DermaTAF, Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
