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    NDC 00054-0472-21 Everolimus 0.75 mg/1 Details

    Everolimus 0.75 mg/1

    Everolimus is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 00054-0472
    Product ID 0054-0472_9b85d4ee-2847-4f7b-ad84-8342e3e8b66f
    Associated GPIs 99404035000330
    GCN Sequence Number 059249
    GCN Sequence Number Description everolimus TABLET 0.75 MG ORAL
    HIC3 Z2E
    HIC3 Description IMMUNOSUPPRESSIVES
    GCN 24827
    HICL Sequence Number 032975
    HICL Sequence Number Description EVEROLIMUS
    Brand/Generic Generic
    Proprietary Name Everolimus
    Proprietary Name Suffix n/a
    Non-Proprietary Name Everolimus
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 0.75
    Active Ingredient Units mg/1
    Substance Name EVEROLIMUS
    Labeler Name Hikma Pharmaceuticals USA Inc.
    Pharmaceutical Class Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206133
    Listing Certified Through 2024-12-31

    Package

    NDC 00054-0472-21 (00054047221)

    NDC Package Code 0054-0472-21
    Billing NDC 00054047221
    Package 60 TABLET in 1 BOTTLE (0054-0472-21)
    Marketing Start Date 2020-03-10
    NDC Exclude Flag N
    Pricing Information N/A