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    NDC 71335-1713-09 Hydrochlorothiazide 12.5 mg/1 Details

    Hydrochlorothiazide 12.5 mg/1

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

    Product Information

    NDC 71335-1713
    Product ID 71335-1713_fd64e438-d644-c531-e053-6294a90a703c
    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 CAPSULE
    Route ORAL
    Active Ingredient Strength 12.5
    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 ANDA203561
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1713-09 (71335171309)

    NDC Package Code 71335-1713-9
    Billing NDC 71335171309
    Package 14 CAPSULE in 1 BOTTLE (71335-1713-9)
    Marketing Start Date 2021-07-02
    NDC Exclude Flag N
    Pricing Information N/A