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    NDC 63629-1071-01 Spironolactone and Hydrochlorothiazide 25; 25 mg/1; mg/1 Details

    Spironolactone and Hydrochlorothiazide 25; 25 mg/1; mg/1

    Spironolactone and 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; SPIRONOLACTONE.

    Product Information

    NDC 63629-1071
    Product ID 63629-1071_fbfcc5e3-bce7-3305-e053-6394a90a7c2e
    Associated GPIs 37990002200310
    GCN Sequence Number 006813
    GCN Sequence Number Description spironolact/hydrochlorothiazid TABLET 25 MG-25MG ORAL
    HIC3 R1L
    HIC3 Description POTASSIUM SPARING DIURETICS IN COMBINATION
    GCN 82330
    HICL Sequence Number 002900
    HICL Sequence Number Description SPIRONOLACTONE/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Spironolactone and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Spironolactone and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA089534
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-1071-01 (63629107101)

    NDC Package Code 63629-1071-1
    Billing NDC 63629107101
    Package 30 TABLET in 1 BOTTLE, PLASTIC (63629-1071-1)
    Marketing Start Date 2020-09-15
    NDC Exclude Flag N
    Pricing Information N/A