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    NDC 00074-5015-02 Skyrizi 600 mg/10mL Details

    Skyrizi 600 mg/10mL

    Skyrizi is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AbbVie Inc.. The primary component is RISANKIZUMAB.

    Product Information

    NDC 00074-5015
    Product ID 0074-5015_7718dd85-622c-478e-ae9b-91e14a1373c6
    Associated GPIs 52504060702020
    GCN Sequence Number 083490
    GCN Sequence Number Description risankizumab-rzaa VIAL 600MG/10ML INTRAVEN
    HIC3 V4E
    HIC3 Description IL-23 RECEPTOR ANTAGONIST, MONOCLONAL ANTIBODY
    GCN 52473
    HICL Sequence Number 045699
    HICL Sequence Number Description RISANKIZUMAB-RZAA
    Brand/Generic Brand
    Proprietary Name Skyrizi
    Proprietary Name Suffix n/a
    Non-Proprietary Name risankizumab-rzaa
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAVENOUS
    Active Ingredient Strength 600
    Active Ingredient Units mg/10mL
    Substance Name RISANKIZUMAB
    Labeler Name AbbVie Inc.
    Pharmaceutical Class Interleukin-23 Antagonist [EPC], Interleukin-23 Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA761262
    Listing Certified Through 2025-12-31

    Package

    NDC 00074-5015-02 (00074501502)

    NDC Package Code 0074-5015-02
    Billing NDC 00074501502
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0074-5015-02) / 10 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2022-06-16
    NDC Exclude Flag N
    Pricing Information N/A