NDC 0259-4126

Naftin

Naftifine Hydrochloride

Naftin is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Merz Pharmaceuticals, Llc. The primary component is Naftifine Hydrochloride.

Product ID0259-4126_00829a7d-d654-41d1-a4cd-fd61dd93c1fb
NDC0259-4126
Product TypeHuman Prescription Drug
Proprietary NameNaftin
Generic NameNaftifine Hydrochloride
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date1998-06-01
Marketing CategoryNDA / NDA
Application NumberNDA019599
Labeler NameMerz Pharmaceuticals, LLC
Substance NameNAFTIFINE HYDROCHLORIDE
Active Ingredient Strength10 mg/g
Pharm ClassesAllylamine [CS],Allylamine Antifungal [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0259-4126-60

1 TUBE in 1 CARTON (0259-4126-60) > 60 g in 1 TUBE
Marketing Start Date1998-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0259-4126-15 [00259412615]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-06-01
Marketing End Date2013-05-06

NDC 0259-4126-09 [00259412609]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date1998-06-01
Marketing End Date2013-05-06

NDC 0259-4126-60 [00259412660]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date1998-06-01
Inactivation Date2020-01-31

NDC 0259-4126-02 [00259412602]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-01-15
Inactivation Date2020-01-31

NDC 0259-4126-90 [00259412690]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date1998-06-01
Inactivation Date2020-01-31

NDC 0259-4126-04 [00259412604]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-06-01
Marketing End Date2013-05-06

NDC 0259-4126-03 [00259412603]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-06-01
Marketing End Date2013-05-06

NDC 0259-4126-30 [00259412630]

Naftin CREAM
Marketing CategoryNDA
Application NumberNDA019599
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date1998-06-01
Marketing End Date2013-05-06

Drug Details

Active Ingredients

IngredientStrength
NAFTIFINE HYDROCHLORIDE10 mg/g

OpenFDA Data

SPL SET ID:f4b6c5d8-615c-47d6-8ad9-523c7ab146af
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 896112
  • 896110

    • Pharmacological Class

    • Allylamine [CS]
    • Allylamine Antifungal [EPC]

    NDC Crossover Matching brand name "Naftin" or generic name "Naftifine Hydrochloride"

    NDCBrand NameGeneric Name
    0259-4126NaftinNAFTIFINE HYDROCHLORIDE
    54766-102NaftinNaftifine Hydrochloride
    54766-770NaftinNAFTIFINE HYDROCHLORIDE
    54766-772NaftinNaftifine Hydrochloride
    0115-1510NAFTIFINE HYDROCHLORIDENAFTIFINE HYDROCHLORIDE
    0115-1512NAFTIFINE HYDROCHLORIDENAFTIFINE HYDROCHLORIDE
    40085-201Naftifine HydrochlorideNAFTIFINE HYDROCHLORIDE
    40085-203Naftifine HydrochlorideNAFTIFINE HYDROCHLORIDE
    51672-1362Naftifine HydrochlorideNaftifine Hydrochloride
    51672-1368Naftifine HydrochlorideNaftifine Hydrochloride
    51672-1376Naftifine HydrochlorideNaftifine Hydrochloride
    70700-161Naftifine hydrochlorideNaftifine hydrochloride

    Trademark Results [Naftin]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    NAFTIN
    NAFTIN
    73706755 not registered Dead/Abandoned
    THAMES PHARMACAL CO., INC.
    1988-01-21
    NAFTIN
    NAFTIN
    73589735 1412990 Live/Registered
    ALLERGAN PHARMACEUTICALS, INC.
    1986-03-24
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