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    NDC 33342-0175-44 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, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Macleods Pharmaceuticals Limited. The primary component is HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 33342-0175
    Product ID 33342-175_03ff0f7e-6aa1-4c38-8c9a-5f1c6a56c747
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25; 40
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
    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 ANDA204801
    Listing Certified Through 2024-12-31

    Package

    NDC 33342-0175-44 (33342017544)

    NDC Package Code 33342-175-44
    Billing NDC 33342017544
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (33342-175-44)
    Marketing Start Date 2023-06-02
    NDC Exclude Flag N
    Pricing Information N/A