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    NDC 67877-0419-01 Linezolid 600 mg/1 Details

    Linezolid 600 mg/1

    Linezolid is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is LINEZOLID.

    Product Information

    NDC 67877-0419
    Product ID 67877-419_7669ffcf-5e46-4535-a958-a9ec4bc7d065
    Associated GPIs 16230040000330
    GCN Sequence Number 045131
    GCN Sequence Number Description linezolid TABLET 600 MG ORAL
    HIC3 W1O
    HIC3 Description OXAZOLIDINONE ANTIBIOTICS
    GCN 26870
    HICL Sequence Number 021157
    HICL Sequence Number Description LINEZOLID
    Brand/Generic Generic
    Proprietary Name Linezolid
    Proprietary Name Suffix n/a
    Non-Proprietary Name Linezolid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name LINEZOLID
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205517
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0419-01 (67877041901)

    NDC Package Code 67877-419-01
    Billing NDC 67877041901
    Package 100 TABLET, FILM COATED in 1 BOTTLE (67877-419-01)
    Marketing Start Date 2015-12-21
    NDC Exclude Flag N
    Pricing Information N/A