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    NDC 00409-1703-01 BORTEZOMIB 2.5 mg/1 Details

    BORTEZOMIB 2.5 mg/1

    BORTEZOMIB is a INTRAVENOUS; SUBCUTANEOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is BORTEZOMIB.

    Product Information

    NDC 00409-1703
    Product ID 0409-1703_e7c31651-e301-43f9-bc81-e0fd5dcb828c
    Associated GPIs 21536015002113
    GCN Sequence Number 081369
    GCN Sequence Number Description bortezomib VIAL 2.5 MG INJECTION
    HIC3 V1Q
    HIC3 Description ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS
    GCN 48454
    HICL Sequence Number 025202
    HICL Sequence Number Description BORTEZOMIB
    Brand/Generic Generic
    Proprietary Name BORTEZOMIB
    Proprietary Name Suffix n/a
    Non-Proprietary Name BORTEZOMIB
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name BORTEZOMIB
    Labeler Name Hospira, Inc.
    Pharmaceutical Class Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209191
    Listing Certified Through 2024-12-31

    Package

    NDC 00409-1703-01 (00409170301)

    NDC Package Code 0409-1703-01
    Billing NDC 00409170301
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1703-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2022-05-16
    NDC Exclude Flag N
    Pricing Information N/A