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    NDC 70710-1411-01 BORTEZOMIB 1 mg/mL Details

    BORTEZOMIB 1 mg/mL

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

    Product Information

    NDC 70710-1411
    Product ID 70710-1411_77554fd4-a569-4180-9a5f-e51962f8524b
    Associated GPIs 21536015002120
    GCN Sequence Number 052124
    GCN Sequence Number Description bortezomib VIAL 3.5 MG INJECTION
    HIC3 V1Q
    HIC3 Description ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS
    GCN 19656
    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/mL
    Substance Name BORTEZOMIB
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210204
    Listing Certified Through 2024-12-31

    Package

    NDC 70710-1411-01 (70710141101)

    NDC Package Code 70710-1411-1
    Billing NDC 70710141101
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1411-1) / 3.5 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2022-05-02
    NDC Exclude Flag N
    Pricing Information N/A