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    NDC 00067-3998-42 Lamisil 10 mg/g Details

    Lamisil 10 mg/g

    Lamisil is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is TERBINAFINE HYDROCHLORIDE.

    Product Information

    NDC 00067-3998
    Product ID 0067-3998_f4438d90-0dcc-40ee-92a7-bdceb17ef010
    Associated GPIs 90150087103710
    GCN Sequence Number 018273
    GCN Sequence Number Description terbinafine HCl CREAM (G) 1 % TOPICAL
    HIC3 Q5F
    HIC3 Description TOPICAL ANTIFUNGALS
    GCN 62498
    HICL Sequence Number 007590
    HICL Sequence Number Description TERBINAFINE HCL
    Brand/Generic Brand
    Proprietary Name Lamisil
    Proprietary Name Suffix AT
    Non-Proprietary Name TERBINAFINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/g
    Substance Name TERBINAFINE HYDROCHLORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Allylamine Antifungal [EPC], Allylamine [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020980
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-3998-42 (00067399842)

    NDC Package Code 0067-3998-42
    Billing NDC 00067399842
    Package 1 TUBE in 1 CARTON (0067-3998-42) / 12 g in 1 TUBE
    Marketing Start Date 2005-08-10
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL de5def4a-f77f-4ea6-a497-24f041c1f123 Details

    Revised: 10/2022