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    NDC 70377-0012-22 EVEROLIMUS 7.5 mg/1 Details

    EVEROLIMUS 7.5 mg/1

    EVEROLIMUS is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Biocon Pharma Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 70377-0012
    Product ID 70377-012_c9b1595f-d199-a6c4-6ca0-c3d1a751c94c
    Associated GPIs 21532530000325
    GCN Sequence Number 068582
    GCN Sequence Number Description everolimus TABLET 7.5 MG ORAL
    HIC3 V3C
    HIC3 Description ANTINEOPLASTIC - MTOR KINASE INHIBITORS
    GCN 31396
    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 7.5
    Active Ingredient Units mg/1
    Substance Name EVEROLIMUS
    Labeler Name Biocon Pharma 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 ANDA214182
    Listing Certified Through 2024-12-31

    Package

    NDC 70377-0012-22 (70377001222)

    NDC Package Code 70377-012-22
    Billing NDC 70377001222
    Package 4 BLISTER PACK in 1 CARTON (70377-012-22) / 7 TABLET in 1 BLISTER PACK
    Marketing Start Date 2021-10-01
    NDC Exclude Flag N
    Pricing Information N/A