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    NDC 00069-3033-20 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 Pfizer Laboratories Div Pfizer Inc. The primary component is DOXORUBICIN HYDROCHLORIDE.

    Product Information

    NDC 00069-3033
    Product ID 0069-3033_0979766c-fbf5-4a1e-a4bc-ea5643527f9a
    Associated GPIs 21200040102010
    GCN Sequence Number 008819
    GCN Sequence Number Description doxorubicin HCl VIAL 2 MG/ML INTRAVEN
    HIC3 V1D
    HIC3 Description ANTIBIOTIC ANTINEOPLASTICS
    GCN 47340
    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 Pfizer Laboratories Div Pfizer Inc
    Pharmaceutical Class Anthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA050629
    Listing Certified Through 2024-12-31

    Package

    NDC 00069-3033-20 (00069303320)

    NDC Package Code 0069-3033-20
    Billing NDC 00069303320
    Package 1 VIAL, MULTI-DOSE in 1 CARTON (0069-3033-20) / 75 mL in 1 VIAL, MULTI-DOSE
    Marketing Start Date 1987-12-23
    NDC Exclude Flag N
    Pricing Information N/A