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    NDC 63629-4093-04 ondansetron hydrochloride 8 mg/1 Details

    ondansetron hydrochloride 8 mg/1

    ondansetron hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 63629-4093
    Product ID 63629-4093_a63e904d-7fac-4b56-9c0d-4642ffe347cf
    Associated GPIs 50250065050320
    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 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 8
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077050
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-4093-04 (63629409304)

    NDC Package Code 63629-4093-4
    Billing NDC 63629409304
    Package 3 TABLET, FILM COATED in 1 BOTTLE (63629-4093-4)
    Marketing Start Date 2009-06-03
    NDC Exclude Flag N
    Pricing Information N/A