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    NDC 62332-0183-91 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 Alembic Pharmaceuticals Inc.. The primary component is LINEZOLID.

    Product Information

    NDC 62332-0183
    Product ID 62332-183_008b01d8-4425-4317-a172-4cc2a9e4e39d
    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 Alembic Pharmaceuticals Inc.
    Pharmaceutical Class Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205233
    Listing Certified Through 2024-12-31

    Package

    NDC 62332-0183-91 (62332018391)

    NDC Package Code 62332-183-91
    Billing NDC 62332018391
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (62332-183-91)
    Marketing Start Date 2015-12-22
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL ca930576-62ab-4af5-ac3e-27ca376baca6 Details

    Revised: 8/2020