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    NDC 00409-1704-01 BORTEZOMIB 1 mg/1 Details

    BORTEZOMIB 1 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 00409-1704
    Product ID 0409-1704_e7c31651-e301-43f9-bc81-e0fd5dcb828c
    Associated GPIs 21536015002110
    GCN Sequence Number 071060
    GCN Sequence Number Description bortezomib VIAL 1 MG INJECTION
    HIC3 V1Q
    HIC3 Description ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS
    GCN 34747
    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 1
    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 00409-1704-01 (00409170401)

    NDC Package Code 0409-1704-01
    Billing NDC 00409170401
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1704-01) / 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