Search by Drug Name or NDC

    NDC 00024-5919-02 Dupixent 200 mg/1.14mL Details

    Dupixent 200 mg/1.14mL

    Dupixent is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by sanofi-aventis U.S. LLC. The primary component is DUPILUMAB.

    Product Information

    NDC 00024-5919
    Product ID 0024-5919_214be693-3f1d-42ee-b72a-f3f210a4ce43
    Associated GPIs 9027302000D215
    GCN Sequence Number 081615
    GCN Sequence Number Description dupilumab PEN INJCTR 200MG/1.14 SUBCUT
    HIC3 V4D
    HIC3 Description INTERLEUKIN-4(IL-4) RECEPTOR ALPHA ANTAGONIST, MAB
    GCN 48785
    HICL Sequence Number 044180
    HICL Sequence Number Description DUPILUMAB
    Brand/Generic Brand
    Proprietary Name Dupixent
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dupilumab
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 200
    Active Ingredient Units mg/1.14mL
    Substance Name DUPILUMAB
    Labeler Name sanofi-aventis U.S. LLC
    Pharmaceutical Class Antibodies, Monoclonal [CS], Interleukin 4 Receptor alpha Antagonists [MoA], Interleukin-4 Receptor alpha Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA761055
    Listing Certified Through 2024-12-31

    Package

    NDC 00024-5919-02 (00024591902)

    NDC Package Code 0024-5919-02
    Billing NDC 00024591902
    Package 2 SYRINGE, GLASS in 1 CARTON (0024-5919-02) / 1.14 mL in 1 SYRINGE, GLASS (0024-5919-00)
    Marketing Start Date 2021-06-14
    NDC Exclude Flag N
    Pricing Information N/A