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    NDC 72789-0162-30 Losartan Potassium and Hydrochlorothiazide 12.5; 50 mg/1; mg/1 Details

    Losartan Potassium and Hydrochlorothiazide 12.5; 50 mg/1; mg/1

    Losartan Potassium and Hydrochlorothiazide is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 72789-0162
    Product ID 72789-162_093046b6-bb71-3239-e063-6294a90af6a8
    Associated GPIs 36994002450320
    GCN Sequence Number 023465
    GCN Sequence Number Description losartan/hydrochlorothiazide TABLET 50-12.5 MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 14852
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 12.5; 50
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name PD-Rx Pharmaceuticals, 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 ANDA201845
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0162-30 (72789016230)

    NDC Package Code 72789-162-30
    Billing NDC 72789016230
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-162-30)
    Marketing Start Date 2021-01-29
    NDC Exclude Flag N
    Pricing Information N/A