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    NDC 65862-0469-10 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, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 65862-0469
    Product ID 65862-469_740ddd9c-172d-4f0f-a8db-f5e1a2add664
    Associated GPIs 36994002450325
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 12.5; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name Aurobindo Pharma Limited
    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 ANDA091629
    Listing Certified Through 2024-12-31

    Package

    NDC 65862-0469-10 (65862046910)

    NDC Package Code 65862-469-10
    Billing NDC 65862046910
    Package 10 BLISTER PACK in 1 CARTON (65862-469-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2010-10-06
    NDC Exclude Flag N
    Pricing Information N/A