Search by Drug Name or NDC

    NDC 10019-0955-01 Cyclophosphamide 500 mg/25mL Details

    Cyclophosphamide 500 mg/25mL

    Cyclophosphamide is a INTRAVENOUS; ORAL INJECTION, POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is CYCLOPHOSPHAMIDE.

    Product Information

    NDC 10019-0955
    Product ID 10019-955_4dc9578a-b1fb-4c0f-9ed5-99b442dbc8f2
    Associated GPIs 21101020002120
    GCN Sequence Number 008769
    GCN Sequence Number Description cyclophosphamide VIAL 500 MG INTRAVEN
    HIC3 V1A
    HIC3 Description ANTINEOPLASTIC - ALKYLATING AGENTS
    GCN 38353
    HICL Sequence Number 003893
    HICL Sequence Number Description CYCLOPHOSPHAMIDE
    Brand/Generic Generic
    Proprietary Name Cyclophosphamide
    Proprietary Name Suffix n/a
    Non-Proprietary Name cyclophosphamide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, FOR SOLUTION
    Route INTRAVENOUS; ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/25mL
    Substance Name CYCLOPHOSPHAMIDE
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Alkylating Activity [MoA], Alkylating Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040745
    Listing Certified Through 2024-12-31

    Package

    NDC 10019-0955-01 (10019095501)

    NDC Package Code 10019-955-01
    Billing NDC 10019095501
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (10019-955-01) / 25 mL in 1 VIAL, SINGLE-DOSE (10019-955-50)
    Marketing Start Date 2008-05-21
    NDC Exclude Flag N
    Pricing Information N/A