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    NDC 51655-0699-53 Ondansetron 4 mg/1 Details

    Ondansetron 4 mg/1

    Ondansetron is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 51655-0699
    Product ID 51655-699_db4da763-1404-63e9-e053-2a95a90a5f0c
    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 Ondansetron
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ondansetron
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 4
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON HYDROCHLORIDE
    Labeler Name Northwind Pharmaceuticals
    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 51655-0699-53 (51655069953)

    NDC Package Code 51655-699-53
    Billing NDC 51655069953
    Package 10 TABLET in 1 BOTTLE, PLASTIC (51655-699-53)
    Marketing Start Date 2021-04-02
    NDC Exclude Flag N
    Pricing Information N/A