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    NDC 71335-0269-01 Hydrochlorothiazide 25 mg/1 Details

    Hydrochlorothiazide 25 mg/1

    Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 71335-0269
    Product ID 71335-0269_fc731fdc-b9af-325f-e053-6294a90a59e4
    Associated GPIs 37600040000305
    GCN Sequence Number 008182
    GCN Sequence Number Description hydrochlorothiazide TABLET 25 MG ORAL
    HIC3 R1F
    HIC3 Description THIAZIDE AND RELATED DIURETICS
    GCN 34824
    HICL Sequence Number 003649
    HICL Sequence Number Description HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name HYDROCHLOROTHIAZIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202556
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0269-01 (71335026901)

    NDC Package Code 71335-0269-1
    Billing NDC 71335026901
    Package 100 TABLET in 1 BOTTLE (71335-0269-1)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A