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    NDC 55513-0842-01 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 55513-0842
    Product ID 55513-842_9e3343fd-826c-41a4-a655-c71b4a651a16
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 55513-0842-01 (55513084201)

    NDC Package Code 55513-842-01
    Billing NDC 55513084201
    Package 1 SYRINGE in 1 CARTON (55513-842-01) / 1 mL in 1 SYRINGE
    Marketing Start Date 2019-03-15
    NDC Exclude Flag N
    Pricing Information N/A