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    NDC 72266-0161-01 Oxaliplatin 5 mg/mL Details

    Oxaliplatin 5 mg/mL

    Oxaliplatin is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by FOSUN PHARMA USA INC.. The primary component is OXALIPLATIN.

    Product Information

    NDC 72266-0161
    Product ID 72266-161_0e7b38b9-5be6-1fad-e063-6294a90a36e3
    Associated GPIs 21100028002025
    GCN Sequence Number 059162
    GCN Sequence Number Description oxaliplatin VIAL 50 MG/10ML INTRAVEN
    HIC3 V1A
    HIC3 Description ANTINEOPLASTIC - ALKYLATING AGENTS
    GCN 24699
    HICL Sequence Number 016687
    HICL Sequence Number Description OXALIPLATIN
    Brand/Generic Generic
    Proprietary Name Oxaliplatin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Oxaliplatin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 5
    Active Ingredient Units mg/mL
    Substance Name OXALIPLATIN
    Labeler Name FOSUN PHARMA USA INC.
    Pharmaceutical Class Platinum-based Drug [EPC], Platinum-containing Compounds [EXT]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207325
    Listing Certified Through 2025-12-31

    Package

    NDC 72266-0161-01 (72266016101)

    NDC Package Code 72266-161-01
    Billing NDC 72266016101
    Package 1 VIAL, SINGLE-USE in 1 CARTON (72266-161-01) / 10 mL in 1 VIAL, SINGLE-USE
    Marketing Start Date 2020-03-30
    NDC Exclude Flag N
    Pricing Information N/A