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    NDC 50090-5450-00 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 A-S Medication Solutions. The primary component is HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 50090-5450
    Product ID 50090-5450_9ee7f46e-a2e2-4486-aa9e-4482ae3b0df2
    Associated GPIs
    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
    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 A-S Medication Solutions
    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 ANDA208847
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5450-00 (50090545000)

    NDC Package Code 50090-5450-0
    Billing NDC 50090545000
    Package 90 TABLET in 1 BOTTLE (50090-5450-0)
    Marketing Start Date 2021-01-25
    NDC Exclude Flag N
    Pricing Information N/A