Search by Drug Name or NDC

    NDC 29300-0192-13 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 Unichem Pharmaceuticals (USA), Inc.. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 29300-0192
    Product ID 29300-192_e82b93f5-8b37-4327-81f9-0cbfcf3d29ac
    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 Unichem Pharmaceuticals (USA), 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 ANDA204832
    Listing Certified Through 2024-12-31

    Package

    NDC 29300-0192-13 (29300019213)

    NDC Package Code 29300-192-13
    Billing NDC 29300019213
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-13)
    Marketing Start Date 2018-01-15
    NDC Exclude Flag N
    Pricing Information N/A