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    NDC 63629-7282-01 Valsartan and Hydrochlorothiazide 12.5; 320 mg/1; mg/1 Details

    Valsartan and Hydrochlorothiazide 12.5; 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 Bryant Ranch Prepack. The primary component is HYDROCHLOROTHIAZIDE; VALSARTAN.

    Product Information

    NDC 63629-7282
    Product ID 63629-7282_5cc6eb0a-e2be-4260-ba6d-63149e41eeb2
    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; 320
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
    Labeler Name Bryant Ranch Prepack
    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 63629-7282-01 (63629728201)

    NDC Package Code 63629-7282-1
    Billing NDC 63629728201
    Package 30 TABLET, FILM COATED in 1 BOTTLE (63629-7282-1)
    Marketing Start Date 2017-05-16
    NDC Exclude Flag N
    Pricing Information N/A