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    NDC 70934-0594-30 Valsartan and Hydrochlorothiazide 25; 160 mg/1; mg/1 Details

    Valsartan and Hydrochlorothiazide 25; 160 mg/1; mg/1

    Valsartan and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is HYDROCHLOROTHIAZIDE; VALSARTAN.

    Product Information

    NDC 70934-0594
    Product ID 70934-594_d8da094e-927d-4e0f-e053-2995a90a4c63
    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 Valsartan and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Valsartan and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 160
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0594-30 (70934059430)

    NDC Package Code 70934-594-30
    Billing NDC 70934059430
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-594-30)
    Marketing Start Date 2020-03-05
    NDC Exclude Flag N
    Pricing Information N/A