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    NDC 60760-0636-20 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 St. Mary's Medical Park Pharmacy. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 60760-0636
    Product ID 60760-636_0c069065-d8c6-1d0e-e063-6294a90ab407
    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 St. Mary's Medical Park Pharmacy
    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 60760-0636-20 (60760063620)

    NDC Package Code 60760-636-20
    Billing NDC 60760063620
    Package 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20)
    Marketing Start Date 2018-03-26
    NDC Exclude Flag N
    Pricing Information N/A