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    NDC 70518-3334-00 Ezetimibe 10 mg/1 Details

    Ezetimibe 10 mg/1

    Ezetimibe is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is EZETIMIBE.

    Product Information

    NDC 70518-3334
    Product ID 70518-3334_06c1a044-cb6c-be06-e063-6294a90a6687
    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 Ezetimibe
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ezetimibe
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name EZETIMIBE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203931
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3334-00 (70518333400)

    NDC Package Code 70518-3334-0
    Billing NDC 70518333400
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70518-3334-0)
    Marketing Start Date 2022-01-16
    NDC Exclude Flag N
    Pricing Information N/A