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    NDC 43063-0857-05 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 PD-Rx Pharmaceuticals, Inc.. The primary component is ONDANSETRON.

    Product Information

    NDC 43063-0857
    Product ID 43063-857_f8c4e860-e702-ade2-e053-6394a90a7c03
    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 PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090469
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0857-05 (43063085705)

    NDC Package Code 43063-857-05
    Billing NDC 43063085705
    Package 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-05)
    Marketing Start Date 2018-06-12
    NDC Exclude Flag N
    Pricing Information N/A