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    NDC 51655-0813-54 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 Northwind Pharmaceuticals. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 51655-0813
    Product ID 51655-813_db99c77a-0b02-9da6-e053-2a95a90a5199
    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 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 Northwind Pharmaceuticals
    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 51655-0813-54 (51655081354)

    NDC Package Code 51655-813-54
    Billing NDC 51655081354
    Package 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-813-54)
    Marketing Start Date 2021-06-10
    NDC Exclude Flag N
    Pricing Information N/A