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    NDC 00025-1021-31 ALDACTAZIDE 50; 50 mg/1; mg/1 Details

    ALDACTAZIDE 50; 50 mg/1; mg/1

    ALDACTAZIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is HYDROCHLOROTHIAZIDE; SPIRONOLACTONE.

    Product Information

    NDC 00025-1021
    Product ID 0025-1021_675ddb03-da87-4741-ad30-31653d578e39
    Associated GPIs 37990002200320
    GCN Sequence Number 006814
    GCN Sequence Number Description spironolact/hydrochlorothiazid TABLET 50 MG-50MG ORAL
    HIC3 R1L
    HIC3 Description POTASSIUM SPARING DIURETICS IN COMBINATION
    GCN 82331
    HICL Sequence Number 002900
    HICL Sequence Number Description SPIRONOLACTONE/HYDROCHLOROTHIAZIDE
    Brand/Generic Brand
    Proprietary Name ALDACTAZIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name spironolactone and hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 50; 50
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
    Labeler Name Pfizer Laboratories Div Pfizer Inc
    Pharmaceutical Class Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA012616
    Listing Certified Through 2024-12-31

    Package

    NDC 00025-1021-31 (00025102131)

    NDC Package Code 0025-1021-31
    Billing NDC 00025102131
    Package 100 TABLET, FILM COATED in 1 BOTTLE (0025-1021-31)
    Marketing Start Date 1978-01-01
    NDC Exclude Flag N
    Pricing Information N/A