Search by Drug Name or NDC

    NDC 70121-1218-07 Doxorubicin Hydrochloride 2 mg/mL Details

    Doxorubicin Hydrochloride 2 mg/mL

    Doxorubicin Hydrochloride is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is DOXORUBICIN HYDROCHLORIDE.

    Product Information

    NDC 70121-1218
    Product ID 70121-1218_7ae0f211-f911-4fa7-96e1-8d77f5f943d9
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Doxorubicin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxorubicin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 2
    Active Ingredient Units mg/mL
    Substance Name DOXORUBICIN HYDROCHLORIDE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Anthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208888
    Listing Certified Through 2024-12-31

    Package

    NDC 70121-1218-07 (70121121807)

    NDC Package Code 70121-1218-7
    Billing NDC 70121121807
    Package 10 CARTON in 1 CARTON (70121-1218-7) / 1 VIAL in 1 CARTON (70121-1218-1) / 10 mL in 1 VIAL
    Marketing Start Date 2017-02-17
    NDC Exclude Flag N
    Pricing Information N/A