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    NDC 50090-3701-00 Olmesartan Medoxomil and Hydrochlorothiazide 12.5; 20 mg/1; mg/1 Details

    Olmesartan Medoxomil and Hydrochlorothiazide 12.5; 20 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 A-S Medication Solutions. The primary component is HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 50090-3701
    Product ID 50090-3701_c3147fdf-8496-4034-828b-c3e5a7e90534
    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 12.5; 20
    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 ANDA205391
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-3701-00 (50090370100)

    NDC Package Code 50090-3701-0
    Billing NDC 50090370100
    Package 30 TABLET, FILM COATED in 1 BOTTLE (50090-3701-0)
    Marketing Start Date 2019-10-09
    NDC Exclude Flag N
    Pricing Information N/A