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    NDC 55513-0843-00 AIMOVIG 140 mg/mL Details

    AIMOVIG 140 mg/mL

    AIMOVIG is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amgen Inc. The primary component is ERENUMAB.

    Product Information

    NDC 55513-0843
    Product ID 55513-843_9e3343fd-826c-41a4-a655-c71b4a651a16
    Associated GPIs 6770202010D540
    GCN Sequence Number 079588
    GCN Sequence Number Description erenumab-aooe AUTO INJCT 140 MG/ML SUBCUT
    HIC3 H3F
    HIC3 Description ANTIMIGRAINE PREPARATIONS
    GCN 46116
    HICL Sequence Number 044923
    HICL Sequence Number Description ERENUMAB-AOOE
    Brand/Generic Brand
    Proprietary Name AIMOVIG
    Proprietary Name Suffix n/a
    Non-Proprietary Name erenumab-aooe
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 140
    Active Ingredient Units mg/mL
    Substance Name ERENUMAB
    Labeler Name Amgen Inc
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA761077
    Listing Certified Through 2024-12-31

    Package

    NDC 55513-0843-00 (55513084300)

    NDC Package Code 55513-843-00
    Billing NDC 55513084300
    Package 1 SYRINGE in 1 CARTON (55513-843-00) / 1 mL in 1 SYRINGE
    Marketing Start Date 2019-03-15
    NDC Exclude Flag N
    Pricing Information N/A