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    NDC 00093-7768-24 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 Teva Pharmaceuticals USA, Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 00093-7768
    Product ID 0093-7768_6595b273-ae65-4945-898d-f4c0d06991e5
    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 Teva 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 ANDA210050
    Listing Certified Through 2024-12-31

    Package

    NDC 00093-7768-24 (00093776824)

    NDC Package Code 0093-7768-24
    Billing NDC 00093776824
    Package 28 BLISTER PACK in 1 CARTON (0093-7768-24) / 1 TABLET in 1 BLISTER PACK (0093-7768-19)
    Marketing Start Date 2020-06-10
    NDC Exclude Flag N
    Pricing Information N/A