Product NDC: | 0259-4770 |
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) |
Product NDC: | 0259-4770 |
Labeler Name: | Merz Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019356 |
Marketing Category: | NDA |
Start Marketing Date: | 19901001 |
Package NDC: | 0259-4770-60 |
Package Description: | 1 TUBE in 1 CARTON (0259-4770-60) > 60 g in 1 TUBE |
NDC Code | 0259-4770-60 |
Proprietary Name | Naftin |
Package Description | 1 TUBE in 1 CARTON (0259-4770-60) > 60 g in 1 TUBE |
Product NDC | 0259-4770 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NAFTIFINE HYDROCHLORIDE |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 19901001 |
Marketing Category Name | NDA |
Labeler Name | Merz Pharmaceuticals, LLC |
Substance Name | NAFTIFINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |