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    NDC 71335-0145-02 Hydrochlorothiazide 50 mg/1 Details

    Hydrochlorothiazide 50 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 71335-0145
    Product ID 71335-0145_fc734abf-2064-6c02-e053-6394a90a1637
    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 Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    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 71335-0145-02 (71335014502)

    NDC Package Code 71335-0145-2
    Billing NDC 71335014502
    Package 60 TABLET in 1 BOTTLE (71335-0145-2)
    Marketing Start Date 2019-05-21
    NDC Exclude Flag N
    Pricing Information N/A