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    NDC 50242-0080-88 LUCENTIS 10 mg/mL Details

    LUCENTIS 10 mg/mL

    LUCENTIS is a INTRAVITREAL INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Genentech, Inc.. The primary component is RANIBIZUMAB.

    Product Information

    NDC 50242-0080
    Product ID 50242-080_bff71896-6094-485b-a864-50c1ff847faa
    Associated GPIs 86655060002020 8665506000E520
    GCN Sequence Number 061119
    GCN Sequence Number Description ranibizumab VIAL 0.5MG/0.05 INTRAOCULR
    HIC3 Q2F
    HIC3 Description OPHTH. VEGF-A RECEPTOR ANTAG. RCMB MC ANTIBODY
    GCN 27289
    HICL Sequence Number 033861
    HICL Sequence Number Description RANIBIZUMAB
    Brand/Generic Brand
    Proprietary Name LUCENTIS
    Proprietary Name Suffix n/a
    Non-Proprietary Name RANIBIZUMAB
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVITREAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/mL
    Substance Name RANIBIZUMAB
    Labeler Name Genentech, Inc.
    Pharmaceutical Class Vascular Endothelial Growth Factor Inhibitor [EPC], Vascular Endothelial Growth Factor Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA125156
    Listing Certified Through 2024-12-31

    Package

    NDC 50242-0080-88 (50242008088)

    NDC Package Code 50242-080-88
    Billing NDC 50242008088
    Package 1 SYRINGE, GLASS in 1 CARTON (50242-080-88) / .05 mL in 1 SYRINGE, GLASS
    Marketing Start Date 2016-10-13
    NDC Exclude Flag N
    Pricing Information N/A