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    NDC 70121-1238-01 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 Amneal Pharmaceuticals LLC. The primary component is CYCLOPHOSPHAMIDE.

    Product Information

    NDC 70121-1238
    Product ID 70121-1238_34a01262-75d3-4c57-baad-2f6d4c0ca8c3
    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 Amneal Pharmaceuticals LLC
    Pharmaceutical Class Alkylating Activity [MoA], Alkylating Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210046
    Listing Certified Through 2024-12-31

    Package

    NDC 70121-1238-01 (70121123801)

    NDC Package Code 70121-1238-1
    Billing NDC 70121123801
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1238-1) / 25 mL in 1 VIAL, SINGLE-DOSE
    Marketing Start Date 2018-05-31
    NDC Exclude Flag N
    Pricing Information N/A