Search by Drug Name or NDC

    NDC 47783-0645-01 TAKHZYRO 150 mg/mL Details

    TAKHZYRO 150 mg/mL

    TAKHZYRO is a SUBCUTANEOUS SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Takeda Pharmaceuticals America, Inc.. The primary component is LANADELUMAB.

    Product Information

    NDC 47783-0645
    Product ID 47783-645_7b67bee7-cd75-431e-949e-39399e849426
    Associated GPIs
    GCN Sequence Number 084405
    GCN Sequence Number Description lanadelumab-flyo SYRINGE 150 MG/ML SUBCUT
    HIC3 A7N
    HIC3 Description PLASMA KALLIKREIN INHIBITORS
    GCN 53706
    HICL Sequence Number 045177
    HICL Sequence Number Description LANADELUMAB-FLYO
    Brand/Generic Brand
    Proprietary Name TAKHZYRO
    Proprietary Name Suffix n/a
    Non-Proprietary Name lanadelumab-flyo
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 150
    Active Ingredient Units mg/mL
    Substance Name LANADELUMAB
    Labeler Name Takeda Pharmaceuticals America, Inc.
    Pharmaceutical Class Kallikrein Inhibitors [MoA], Plasma Kallikrein Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA761090
    Listing Certified Through 2024-12-31

    Package

    NDC 47783-0645-01 (47783064501)

    NDC Package Code 47783-645-01
    Billing NDC 47783064501
    Package 1 SYRINGE, GLASS in 1 CARTON (47783-645-01) / 1 mL in 1 SYRINGE, GLASS
    Marketing Start Date 2023-02-03
    NDC Exclude Flag N
    Pricing Information N/A