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    NDC 63629-4014-01 Ondansetron 4 mg/1 Details

    Ondansetron 4 mg/1

    Ondansetron is a ORAL TABLET, ORALLY DISINTEGRATING in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is ONDANSETRON.

    Product Information

    NDC 63629-4014
    Product ID 63629-4014_267abdd4-02f8-c04d-d009-d838f7e0a905
    Associated GPIs 50250065007220
    GCN Sequence Number 041562
    GCN Sequence Number Description ondansetron TAB RAPDIS 4 MG ORAL
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 20045
    HICL Sequence Number 019058
    HICL Sequence Number Description ONDANSETRON
    Brand/Generic Generic
    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 4
    Active Ingredient Units mg/1
    Substance Name ONDANSETRON
    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 ANDA078152
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-4014-01 (63629401401)

    NDC Package Code 63629-4014-1
    Billing NDC 63629401401
    Package 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-4014-1)
    Marketing Start Date 2009-05-29
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 267abdd4-02f8-c04d-d009-d838f7e0a905 Details

    Revised: 12/2021