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    NDC 00143-9241-01 Bleomycin 30 [USP'U]/1 Details

    Bleomycin 30 [USP'U]/1

    Bleomycin is a INTRAMUSCULAR; INTRAPLEURAL; INTRAVENOUS; SUBCUTANEOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is BLEOMYCIN SULFATE.

    Product Information

    NDC 00143-9241
    Product ID 0143-9241_17a59fa2-9e0c-4be6-b9ef-8d1299352a0f
    Associated GPIs 21200010102115
    GCN Sequence Number 026281
    GCN Sequence Number Description bleomycin sulfate VIAL 30 UNIT INJECTION
    HIC3 V1D
    HIC3 Description ANTIBIOTIC ANTINEOPLASTICS
    GCN 38613
    HICL Sequence Number 003918
    HICL Sequence Number Description BLEOMYCIN SULFATE
    Brand/Generic Generic
    Proprietary Name Bleomycin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bleomycin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAMUSCULAR; INTRAPLEURAL; INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 30
    Active Ingredient Units [USP'U]/1
    Substance Name BLEOMYCIN SULFATE
    Labeler Name Hikma Pharmaceuticals USA Inc.
    Pharmaceutical Class Cytoprotective Agent [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065042
    Listing Certified Through 2024-12-31

    Package

    NDC 00143-9241-01 (00143924101)

    NDC Package Code 0143-9241-01
    Billing NDC 00143924101
    Package 1 VIAL in 1 BOX, UNIT-DOSE (0143-9241-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
    Marketing Start Date 2018-01-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cccfb763-79fa-4186-89fb-d8d061d3c161 Details

    Revised: 4/2022