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    NDC 68788-7565-03 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 Preferred Pharmaceuticals, Inc.. The primary component is ONDANSETRON.

    Product Information

    NDC 68788-7565
    Product ID 68788-7565_0cd5ffc6-20fb-4e0d-bcc3-c799271ed0de
    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 Preferred Pharmaceuticals, Inc.
    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 68788-7565-03 (68788756503)

    NDC Package Code 68788-7565-3
    Billing NDC 68788756503
    Package 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7565-3)
    Marketing Start Date 2019-12-27
    NDC Exclude Flag N
    Pricing Information N/A