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    NDC 13668-0253-01 OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE 25; 40 mg/1; mg/1 Details

    OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE 25; 40 mg/1; mg/1

    OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 13668-0253
    Product ID 13668-253_59f9a4b5-5fca-4aa0-9fc4-6ae1ea1d560e
    Associated GPIs 36994002500345
    GCN Sequence Number 052835
    GCN Sequence Number Description olmesartan/hydrochlorothiazide TABLET 40 MG-25MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 20076
    HICL Sequence Number 025446
    HICL Sequence Number Description OLMESARTAN MEDOXOMIL/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE 40/25
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
    Labeler Name Torrent 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 ANDA206515
    Listing Certified Through n/a

    Package

    NDC 13668-0253-01 (13668025301)

    NDC Package Code 13668-253-01
    Billing NDC 13668025301
    Package 1000 TABLET in 1 BOTTLE (13668-253-01)
    Marketing Start Date 2017-04-24
    NDC Exclude Flag N
    Pricing Information N/A