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    NDC 00409-0801-01 Nipent 2 mg/mL Details

    Nipent 2 mg/mL

    Nipent is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is PENTOSTATIN.

    Product Information

    NDC 00409-0801
    Product ID 0409-0801_d0a07732-fd08-4f3e-bbc8-cb039f6b9026
    Associated GPIs 21700045002120
    GCN Sequence Number 016510
    GCN Sequence Number Description pentostatin VIAL 10 MG INTRAVEN
    HIC3 V1B
    HIC3 Description ANTINEOPLASTIC - ANTIMETABOLITES
    GCN 19901
    HICL Sequence Number 006301
    HICL Sequence Number Description PENTOSTATIN
    Brand/Generic Brand
    Proprietary Name Nipent
    Proprietary Name Suffix n/a
    Non-Proprietary Name PENTOSTATIN
    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 PENTOSTATIN
    Labeler Name Hospira, Inc.
    Pharmaceutical Class Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020122
    Listing Certified Through 2024-12-31

    Package

    NDC 00409-0801-01 (00409080101)

    NDC Package Code 0409-0801-01
    Billing NDC 00409080101
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0801-01) / 5 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2007-08-15
    NDC Exclude Flag N
    Pricing Information N/A