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    NDC 00310-4700-01 LUMOXITI 1 mg/mL Details

    LUMOXITI 1 mg/mL

    LUMOXITI is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AstraZeneca Pharmaceuticals LP. The primary component is MOXETUMOMAB PASUDOTOX.

    Product Information

    NDC 00310-4700
    Product ID 0310-4700_bd80307f-5490-4eda-a787-423a7ca788cc
    Associated GPIs 21352236502120
    GCN Sequence Number 079139
    GCN Sequence Number Description moxetumomab pasudotox-tdfk VIAL 1 MG INTRAVEN
    HIC3 V38
    HIC3 Description ANTINEOPLASTIC-CD22 DIRECT ANTIBODY/CYTOTOXIN CONJ
    GCN 45585
    HICL Sequence Number 045363
    HICL Sequence Number Description MOXETUMOMAB PASUDOTOX-TDFK
    Brand/Generic Brand
    Proprietary Name LUMOXITI
    Proprietary Name Suffix n/a
    Non-Proprietary Name moxetumomab pasudotox
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 1
    Active Ingredient Units mg/mL
    Substance Name MOXETUMOMAB PASUDOTOX
    Labeler Name AstraZeneca Pharmaceuticals LP
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA761104
    Listing Certified Through n/a

    Package

    NDC 00310-4700-01 (00310470001)

    NDC Package Code 0310-4700-01
    Billing NDC 00310470001
    Package 1 VIAL in 1 CARTON (0310-4700-01) / 1 mL in 1 VIAL
    Marketing Start Date 2018-10-24
    NDC Exclude Flag N
    Pricing Information N/A