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    NDC 70518-2578-01 Losartan Potassium and Hydrochlorothiazide 25; 100 mg/1; mg/1 Details

    Losartan Potassium and Hydrochlorothiazide 25; 100 mg/1; mg/1

    Losartan Potassium and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 70518-2578
    Product ID 70518-2578_0d1ee8af-564f-327e-e063-6394a90a0f8f
    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 Losartan Potassium and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Losartan Potassium and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078245
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2578-01 (70518257801)

    NDC Package Code 70518-2578-1
    Billing NDC 70518257801
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70518-2578-1)
    Marketing Start Date 2020-04-08
    NDC Exclude Flag N
    Pricing Information N/A