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    NDC 33342-0052-12 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, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Macleods Pharmaceuticals Limited. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 33342-0052
    Product ID 33342-052_6e1eca59-3423-4834-89c7-e776c53e53da
    Associated GPIs 36994002450340
    GCN Sequence Number 040923
    GCN Sequence Number Description losartan/hydrochlorothiazide TABLET 100MG-25MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 14854
    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 25; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name Macleods Pharmaceuticals 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 ANDA202289
    Listing Certified Through 2024-12-31

    Package

    NDC 33342-0052-12 (33342005212)

    NDC Package Code 33342-052-12
    Billing NDC 33342005212
    Package 10 BLISTER PACK in 1 CARTON (33342-052-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2012-09-10
    NDC Exclude Flag N
    Pricing Information N/A