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    NDC 00378-0007-85 Everolimus 5 mg/1 Details

    Everolimus 5 mg/1

    Everolimus is a ORAL TABLET, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 00378-0007
    Product ID 0378-0007_129ab1eb-61df-49de-953c-fca0f0a28eee
    Associated GPIs 21532530007340
    GCN Sequence Number 070921
    GCN Sequence Number Description everolimus TAB SUSP 5 MG ORAL
    HIC3 V3C
    HIC3 Description ANTINEOPLASTIC - MTOR KINASE INHIBITORS
    GCN 34592
    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, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name EVEROLIMUS
    Labeler Name Mylan Pharmaceuticals 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 ANDA210130
    Listing Certified Through 2024-12-31

    Package

    NDC 00378-0007-85 (00378000785)

    NDC Package Code 0378-0007-85
    Billing NDC 00378000785
    Package 4 BLISTER PACK in 1 CARTON (0378-0007-85) / 7 TABLET, FOR SUSPENSION in 1 BLISTER PACK
    Marketing Start Date 2021-10-01
    NDC Exclude Flag N
    Pricing Information N/A