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    NDC 69339-0172-05 Ondansetron 8 mg/1 Details

    Ondansetron 8 mg/1

    Ondansetron is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Natco Pharma USA LLC. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 69339-0172
    Product ID 69339-172_6d27f218-e964-4ae5-8dc7-fa8b4bda500f
    Associated GPIs
    GCN Sequence Number 016393
    GCN Sequence Number Description ondansetron HCl TABLET 8 MG ORAL
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 20042
    HICL Sequence Number 006055
    HICL Sequence Number Description ONDANSETRON HCL
    Brand/Generic Generic
    Proprietary Name Ondansetron
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ondansetron
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 8
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON HYDROCHLORIDE
    Labeler Name Natco Pharma USA LLC
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077851
    Listing Certified Through 2024-12-31

    Package

    NDC 69339-0172-05 (69339017205)

    NDC Package Code 69339-172-05
    Billing NDC 69339017205
    Package 500 TABLET in 1 BOTTLE (69339-172-05)
    Marketing Start Date 2022-10-24
    NDC Exclude Flag N
    Pricing Information N/A