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    NDC 00071-5212-23 ACCURETIC 12.5; 20 mg/1; mg/1 Details

    ACCURETIC 12.5; 20 mg/1; mg/1

    ACCURETIC is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Parke-Davis Div of Pfizer Inc. The primary component is HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE.

    Product Information

    NDC 00071-5212
    Product ID 0071-5212_489727cb-429e-4f04-a973-ae4dc7898519
    Associated GPIs 36991802650330
    GCN Sequence Number 024002
    GCN Sequence Number Description quinapril/hydrochlorothiazide TABLET 20-12.5 MG ORAL
    HIC3 A4J
    HIC3 Description ACE INHIBITOR-THIAZIDE OR THIAZIDE-LIKE DIURETIC
    GCN 54161
    HICL Sequence Number 007826
    HICL Sequence Number Description QUINAPRIL HCL/HYDROCHLOROTHIAZIDE
    Brand/Generic Brand
    Proprietary Name ACCURETIC
    Proprietary Name Suffix n/a
    Non-Proprietary Name quinapril and hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 12.5; 20
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
    Labeler Name Parke-Davis Div of Pfizer Inc
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020125
    Listing Certified Through 2024-12-31

    Package

    NDC 00071-5212-23 (00071521223)

    NDC Package Code 0071-5212-23
    Billing NDC 00071521223
    Package 90 TABLET, FILM COATED in 1 BOTTLE (0071-5212-23)
    Marketing Start Date 2021-12-06
    NDC Exclude Flag N
    Pricing Information N/A