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    NDC 50090-5345-00 Valsartan and Hydrochlorothiazide 25; 320 mg/1; mg/1 Details

    Valsartan and Hydrochlorothiazide 25; 320 mg/1; mg/1

    Valsartan 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; VALSARTAN.

    Product Information

    NDC 50090-5345
    Product ID 50090-5345_48d61518-d6f5-4b1e-8d5f-88cdd766a17d
    Associated GPIs
    GCN Sequence Number 060780
    GCN Sequence Number Description valsartan/hydrochlorothiazide TABLET 320MG-25MG ORAL
    HIC3 A4I
    HIC3 Description ANGIOTENSIN RECEPTOR ANTAG.-THIAZIDE DIURETIC COMB
    GCN 27014
    HICL Sequence Number 017084
    HICL Sequence Number Description VALSARTAN/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Valsartan and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Valsartan and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25; 320
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
    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 ANDA203145
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5345-00 (50090534500)

    NDC Package Code 50090-5345-0
    Billing NDC 50090534500
    Package 90 TABLET, FILM COATED in 1 BOTTLE (50090-5345-0)
    Marketing Start Date 2020-11-05
    NDC Exclude Flag N
    Pricing Information N/A