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    NDC 65862-0208-04 Ondansetron 4 mg/5mL Details

    Ondansetron 4 mg/5mL

    Ondansetron is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is ONDANSETRON HYDROCHLORIDE.

    Product Information

    NDC 65862-0208
    Product ID 65862-208_380686e7-c045-42ef-86c6-0f20b80202b1
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ondansetron Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 4
    Active Ingredient Units mg/5mL
    Substance Name ONDANSETRON HYDROCHLORIDE
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078776
    Listing Certified Through 2024-12-31

    Package

    NDC 65862-0208-04 (65862020804)

    NDC Package Code 65862-208-04
    Billing NDC 65862020804
    Package 1 BOTTLE, PLASTIC in 1 CARTON (65862-208-04) / 50 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2007-11-28
    NDC Exclude Flag N
    Pricing Information N/A