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    NDC 68788-7648-06 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 Preferred Pharmaceuticals, Inc.. The primary component is HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 68788-7648
    Product ID 68788-7648_4473965a-1848-4900-bf32-24c6c1a90318
    Associated GPIs 37600040000305
    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 25
    Active Ingredient Units mg/1
    Substance Name HYDROCHLOROTHIAZIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA085182
    Listing Certified Through 2022-12-31

    Package

    NDC 68788-7648-06 (68788764806)

    NDC Package Code 68788-7648-6
    Billing NDC 68788764806
    Package 60 TABLET in 1 BOTTLE (68788-7648-6)
    Marketing Start Date 2020-04-17
    NDC Exclude Flag N
    Pricing Information N/A