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    NDC 50090-3178-04 Ondansetron Hydrochloride 4 mg/1 Details

    Ondansetron Hydrochloride 4 mg/1

    Ondansetron Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 50090-3178
    Product ID 50090-3178_f74fee7b-ae98-4fbb-84fb-23cd573e3936
    Associated GPIs 50250065050310
    GCN Sequence Number 016392
    GCN Sequence Number Description ondansetron HCl TABLET 4 MG ORAL
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 20041
    HICL Sequence Number 006055
    HICL Sequence Number Description ONDANSETRON HCL
    Brand/Generic Generic
    Proprietary Name Ondansetron Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ondansetron Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 4
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON HYDROCHLORIDE
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078539
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-3178-04 (50090317804)

    NDC Package Code 50090-3178-4
    Billing NDC 50090317804
    Package 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3178-4)
    Marketing Start Date 2014-11-28
    NDC Exclude Flag N
    Pricing Information N/A