Search by Drug Name or NDC

    NDC 55513-0840-01 AIMOVIG 70 mg/mL Details

    AIMOVIG 70 mg/mL

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

    Product Information

    NDC 55513-0840
    Product ID 55513-840_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
    Route SUBCUTANEOUS
    Active Ingredient Strength 70
    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 55513-0840-01 (55513084001)

    NDC Package Code 55513-840-01
    Billing NDC 55513084001
    Package 1 SYRINGE, GLASS in 1 CARTON (55513-840-01) / 1 mL in 1 SYRINGE, GLASS
    Marketing Start Date 2018-05-22
    NDC Exclude Flag N
    Pricing Information N/A