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    NDC 50742-0519-02 CYCLOPHOSPHAMIDE 200 mg/mL Details

    CYCLOPHOSPHAMIDE 200 mg/mL

    CYCLOPHOSPHAMIDE is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ingenus Pharmaceuticals, LLC. The primary component is CYCLOPHOSPHAMIDE ANHYDROUS.

    Product Information

    NDC 50742-0519
    Product ID 50742-519_da2e589c-8946-4193-8543-6d26c05fc48a
    Associated GPIs 21101020002020
    GCN Sequence Number 081349
    GCN Sequence Number Description cyclophosphamide VIAL 200 MG/ML INTRAVEN
    HIC3 V1A
    HIC3 Description ANTINEOPLASTIC - ALKYLATING AGENTS
    GCN 48433
    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, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 200
    Active Ingredient Units mg/mL
    Substance Name CYCLOPHOSPHAMIDE ANHYDROUS
    Labeler Name Ingenus Pharmaceuticals, LLC
    Pharmaceutical Class Alkylating Activity [MoA], Alkylating Drug [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA212501
    Listing Certified Through 2024-12-31

    Package

    NDC 50742-0519-02 (50742051902)

    NDC Package Code 50742-519-02
    Billing NDC 50742051902
    Package 1 VIAL in 1 CARTON (50742-519-02) / 2.5 mL in 1 VIAL
    Marketing Start Date 2020-07-30
    NDC Exclude Flag N
    Pricing Information N/A