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TOLNAFTATE ANTIFUNGAL
TOLNAFTATE ANTIFUNGAL - 0904-0726-45 - (TOLNAFTATE)
Drug Information of TOLNAFTATE ANTIFUNGAL
| Product NDC: | 0904-0726 |
| Proprietary Name: | TOLNAFTATE ANTIFUNGAL |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | .45 g/45g & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TOLNAFTATE ANTIFUNGAL
| Product NDC: | 0904-0726 |
| Labeler Name: | MAJOR Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111101 |
Package Information of TOLNAFTATE ANTIFUNGAL
| Package NDC: | 0904-0726-45 |
| Package Description: | 45 g in 1 BOTTLE, DISPENSING (0904-0726-45) |
NDC Information of TOLNAFTATE ANTIFUNGAL
| NDC Code | 0904-0726-45 |
| Proprietary Name | TOLNAFTATE ANTIFUNGAL |
| Package Description | 45 g in 1 BOTTLE, DISPENSING (0904-0726-45) |
| Product NDC | 0904-0726 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MAJOR Pharmaceuticals Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | .45 |
| Strength Unit | g/45g |
| Pharmaceutical Classes |
