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    NDC 51655-0809-87 Ondansetron 8 mg/1 Details

    Ondansetron 8 mg/1

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

    Product Information

    NDC 51655-0809
    Product ID 51655-809_f708b983-1314-b571-e053-6294a90ad39a
    Associated GPIs 50250065007240
    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, ORALLY DISINTEGRATING
    Route ORAL
    Active Ingredient Strength 8
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090469
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0809-87 (51655080987)

    NDC Package Code 51655-809-87
    Billing NDC 51655080987
    Package 6 TABLET, ORALLY DISINTEGRATING in 1 BAG (51655-809-87)
    Marketing Start Date 2020-11-30
    NDC Exclude Flag N
    Pricing Information N/A