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    NDC 51991-0381-60 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 Breckenridge Pharmaceutical, Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 51991-0381
    Product ID 51991-381_36e34f3e-8f18-4a48-9380-da4029f706a9
    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 tablets
    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 Breckenridge Pharmaceutical, 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 ANDA205432
    Listing Certified Through 2024-12-31

    Package

    NDC 51991-0381-60 (51991038160)

    NDC Package Code 51991-381-60
    Billing NDC 51991038160
    Package 60 BLISTER PACK in 1 CARTON (51991-381-60) / 10 TABLET in 1 BLISTER PACK (51991-381-99)
    Marketing Start Date 2021-05-21
    NDC Exclude Flag N
    Pricing Information N/A