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    NDC 76420-0217-06 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 Asclemed USA, Inc.. The primary component is ONDANSETRON.

    Product Information

    NDC 76420-0217
    Product ID 76420-217_00388f2a-013b-518d-e063-6294a90af1a0
    Associated GPIs
    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 Asclemed USA, 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 76420-0217-06 (76420021706)

    NDC Package Code 76420-217-06
    Billing NDC 76420021706
    Package 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76420-217-06)
    Marketing Start Date 2022-07-20
    NDC Exclude Flag N
    Pricing Information N/A