Naftin - 0259-1102-45 - (Naftifine Hydrochloride)

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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]

Complete Information of Naftin


General Information