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Naftin
Naftin - 54868-2185-2 - (naftifine hydrochloride)
Drug Information of Naftin
| Product NDC: | 54868-2185 |
| Proprietary Name: | Naftin |
| Non Proprietary Name: | naftifine hydrochloride |
| Active Ingredient(s): | 10 mg/g & nbsp; naftifine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naftin
| Product NDC: | 54868-2185 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019356 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051229 |
Package Information of Naftin
| Package NDC: | 54868-2185-2 |
| Package Description: | 1 TUBE in 1 CARTON (54868-2185-2) > 40 g in 1 TUBE |
NDC Information of Naftin
| NDC Code | 54868-2185-2 |
| Proprietary Name | Naftin |
| Package Description | 1 TUBE in 1 CARTON (54868-2185-2) > 40 g in 1 TUBE |
| Product NDC | 54868-2185 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | naftifine hydrochloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20051229 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | NAFTIFINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
