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Tolnaftate
Tolnaftate - 51141-0057-1 - (Tolnaftate)
Drug Information of Tolnaftate
| Product NDC: | 51141-0057 |
| Proprietary Name: | Tolnaftate |
| 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) |
Labeler Information of Tolnaftate
| Product NDC: | 51141-0057 |
| Labeler Name: | NeoPharm Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100827 |
Package Information of Tolnaftate
| Package NDC: | 51141-0057-1 |
| Package Description: | 1 TUBE in 1 BOX (51141-0057-1) > 28 g in 1 TUBE |
NDC Information of Tolnaftate
| NDC Code | 51141-0057-1 |
| Proprietary Name | Tolnaftate |
| Package Description | 1 TUBE in 1 BOX (51141-0057-1) > 28 g in 1 TUBE |
| Product NDC | 51141-0057 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100827 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NeoPharm Co., Ltd. |
| Substance Name | TOLNAFTATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
