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    NDC 53746-0846-90 Valsartan and Hydrochlorothiazide 12.5; 160 mg/1; mg/1 Details

    Valsartan and Hydrochlorothiazide 12.5; 160 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 Amneal Pharmaceuticals of New York LLC. The primary component is HYDROCHLOROTHIAZIDE; VALSARTAN.

    Product Information

    NDC 53746-0846
    Product ID 53746-846_1ed15f09-2051-401f-a320-5f04b85ac8e2
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 12.5; 160
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
    Labeler Name Amneal Pharmaceuticals of New York LLC
    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 ANDA204382
    Listing Certified Through 2024-12-31

    Package

    NDC 53746-0846-90 (53746084690)

    NDC Package Code 53746-846-90
    Billing NDC 53746084690
    Package 90 TABLET, FILM COATED in 1 BOTTLE (53746-846-90)
    Marketing Start Date 2023-08-14
    NDC Exclude Flag N
    Pricing Information N/A