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    NDC 00378-8182-50 OLUX 0.5 mg/g Details

    OLUX 0.5 mg/g

    OLUX is a TOPICAL AEROSOL, FOAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is CLOBETASOL PROPIONATE.

    Product Information

    NDC 00378-8182
    Product ID 0378-8182_aa5310b2-f624-4ac5-bc4a-c907a505d65a
    Associated GPIs 90550025103920
    GCN Sequence Number 046803
    GCN Sequence Number Description clobetasol propionate FOAM 0.05 % TOPICAL
    HIC3 Q5P
    HIC3 Description TOPICAL ANTI-INFLAMMATORY STEROIDAL
    GCN 89743
    HICL Sequence Number 003327
    HICL Sequence Number Description CLOBETASOL PROPIONATE
    Brand/Generic Brand
    Proprietary Name OLUX
    Proprietary Name Suffix n/a
    Non-Proprietary Name clobetasol propionate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form AEROSOL, FOAM
    Route TOPICAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/g
    Substance Name CLOBETASOL PROPIONATE
    Labeler Name Mylan Pharmaceuticals Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021142
    Listing Certified Through 2023-12-31

    Package

    NDC 00378-8182-50 (00378818250)

    NDC Package Code 0378-8182-50
    Billing NDC 00378818250
    Package 50 g in 1 CAN (0378-8182-50)
    Marketing Start Date 2019-04-11
    NDC Exclude Flag N
    Pricing Information N/A