Search by Drug Name or NDC

    NDC 23155-0008-18 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 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is HYDROCHLOROTHIAZIDE.

    Product Information

    NDC 23155-0008
    Product ID 23155-008_5bb598d0-39a7-4bb1-aa1e-e53e7b9a4aec
    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 Heritage Pharmaceuticals Inc. d/b/a Avet 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 2024-12-31

    Package

    NDC 23155-0008-18 (23155000818)

    NDC Package Code 23155-008-18
    Billing NDC 23155000818
    Package 5000 TABLET in 1 BOTTLE (23155-008-18)
    Marketing Start Date 2015-02-01
    NDC Exclude Flag N
    Pricing Information N/A