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    NDC 50090-5113-00 Losartan Potassium and Hydrochlorothiazide 12.5; 100 mg/1; mg/1 Details

    Losartan Potassium and Hydrochlorothiazide 12.5; 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 A-S Medication Solutions. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 50090-5113
    Product ID 50090-5113_0be498b0-382f-4df5-bced-75535404b02b
    Associated GPIs
    GCN Sequence Number 059919
    GCN Sequence Number Description losartan/hydrochlorothiazide TABLET 100-12.5MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 25851
    HICL Sequence Number 009863
    HICL Sequence Number Description LOSARTAN POTASSIUM/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    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 12.5; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name A-S Medication Solutions
    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 50090-5113-00 (50090511300)

    NDC Package Code 50090-5113-0
    Billing NDC 50090511300
    Package 30 TABLET in 1 BOTTLE (50090-5113-0)
    Marketing Start Date 2020-07-30
    NDC Exclude Flag N
    Pricing Information N/A