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Naftin
Naftin - 0259-1102-45 - (Naftifine Hydrochloride)
Drug Information of Naftin
| Product NDC: | 0259-1102 |
| Proprietary Name: | Naftin |
| Non Proprietary Name: | Naftifine Hydrochloride |
| Active Ingredient(s): | 10 mg/2g & nbsp; Naftifine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naftin
| Product NDC: | 0259-1102 |
| Labeler Name: | Merz Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019599 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120301 |
Package Information of Naftin
| Package NDC: | 0259-1102-45 |
| Package Description: | 1 TUBE in 1 CARTON (0259-1102-45) > 45 g in 1 TUBE |
NDC Information of Naftin
| NDC Code | 0259-1102-45 |
| Proprietary Name | Naftin |
| Package Description | 1 TUBE in 1 CARTON (0259-1102-45) > 45 g in 1 TUBE |
| Product NDC | 0259-1102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naftifine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | NDA |
| Labeler Name | Merz Pharmaceuticals, LLC |
| Substance Name | NAFTIFINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/2g |
| Pharmaceutical Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
