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    NDC 49884-0125-91 Everolimus 5 mg/1 Details

    Everolimus 5 mg/1

    Everolimus is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is EVEROLIMUS.

    Product Information

    NDC 49884-0125
    Product ID 49884-125_131a5a57-ee0b-4ee9-9c61-9be3dcdcbb25
    Associated GPIs 21532530000320
    GCN Sequence Number 064994
    GCN Sequence Number Description everolimus TABLET 5 MG ORAL
    HIC3 V3C
    HIC3 Description ANTINEOPLASTIC - MTOR KINASE INHIBITORS
    GCN 20784
    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 5
    Active Ingredient Units mg/1
    Substance Name EVEROLIMUS
    Labeler Name Par 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 ANDA207934
    Listing Certified Through 2024-12-31

    Package

    NDC 49884-0125-91 (49884012591)

    NDC Package Code 49884-125-91
    Billing NDC 49884012591
    Package 28 BLISTER PACK in 1 CARTON (49884-125-91) / 1 TABLET in 1 BLISTER PACK (49884-125-52)
    Marketing Start Date 2019-12-10
    NDC Exclude Flag N
    Pricing Information N/A