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    NDC 68788-9915-03 Ketoconazole 20 mg/g Details

    Ketoconazole 20 mg/g

    Ketoconazole is a TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is KETOCONAZOLE.

    Product Information

    NDC 68788-9915
    Product ID 68788-9915_390b9a29-fdd7-40b2-80b1-f766c1f4e44a
    Associated GPIs 90154045003710
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Ketoconazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ketoconazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/g
    Substance Name KETOCONAZOLE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075638
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-9915-03 (68788991503)

    NDC Package Code 68788-9915-3
    Billing NDC 68788991503
    Package 1 TUBE in 1 CARTON (68788-9915-3) / 30 g in 1 TUBE
    Marketing Start Date 2012-01-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 899a9cb9-09b2-4e16-baa3-058eaab04739 Details

    Revised: 7/2022