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    NDC 57664-0682-30 Linezolid 200 mg/100mL Details

    Linezolid 200 mg/100mL

    Linezolid is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is LINEZOLID.

    Product Information

    NDC 57664-0682
    Product ID 57664-682_aaefa755-b3ef-40d9-b05c-d5a5bda47c1a
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Linezolid
    Proprietary Name Suffix n/a
    Non-Proprietary Name linezolid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 200
    Active Ingredient Units mg/100mL
    Substance Name LINEZOLID
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207354
    Listing Certified Through 2024-12-31

    Package

    NDC 57664-0682-30 (57664068230)

    NDC Package Code 57664-682-30
    Billing NDC 57664068230
    Package 100 mL in 1 BAG (57664-682-30)
    Marketing Start Date 2017-02-01
    NDC Exclude Flag N
    Pricing Information N/A