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    NDC 71335-0067-03 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 71335-0067
    Product ID 71335-0067_3aa6328c-0e31-44a8-885e-8b7717e63906
    Associated GPIs 37600040000110
    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 ANDA090510
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0067-03 (71335006703)

    NDC Package Code 71335-0067-3
    Billing NDC 71335006703
    Package 90 CAPSULE in 1 BOTTLE (71335-0067-3)
    Marketing Start Date 2018-04-03
    NDC Exclude Flag N
    Pricing Information N/A