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    NDC 25021-0207-51 doxorubicin hydrochloride 2 mg/mL Details

    doxorubicin hydrochloride 2 mg/mL

    doxorubicin hydrochloride is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sagent Pharmaceuticals. The primary component is DOXORUBICIN HYDROCHLORIDE.

    Product Information

    NDC 25021-0207
    Product ID 25021-207_ecebeba3-8ead-4c7f-b22c-fdcf977adfe6
    Associated GPIs 21200040102010
    GCN Sequence Number 061483
    GCN Sequence Number Description doxorubicin HCl VIAL 10 MG/5 ML INTRAVEN
    HIC3 V1D
    HIC3 Description ANTIBIOTIC ANTINEOPLASTICS
    GCN 97271
    HICL Sequence Number 003916
    HICL Sequence Number Description DOXORUBICIN HCL
    Brand/Generic Generic
    Proprietary Name doxorubicin hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name doxorubicin hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 2
    Active Ingredient Units mg/mL
    Substance Name DOXORUBICIN HYDROCHLORIDE
    Labeler Name Sagent Pharmaceuticals
    Pharmaceutical Class Anthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209825
    Listing Certified Through 2024-12-31

    Package

    NDC 25021-0207-51 (25021020751)

    NDC Package Code 25021-207-51
    Billing NDC 25021020751
    Package 1 VIAL in 1 CARTON (25021-207-51) / 100 mL in 1 VIAL
    Marketing Start Date 2013-10-31
    NDC Exclude Flag N
    Pricing Information N/A