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    NDC 51655-0415-04 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 Northwind Pharmaceuticals, LLC. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 51655-0415
    Product ID 51655-415_f305c001-ee5a-bef5-e053-2a95a90aafcd
    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 4
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON HYDROCHLORIDE
    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 ANDA078539
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0415-04 (51655041504)

    NDC Package Code 51655-415-04
    Billing NDC 51655041504
    Package 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)
    Marketing Start Date 2018-04-12
    NDC Exclude Flag N
    Pricing Information N/A