NDC 0071-0223

ACCURETIC

Quinapril Hydrochloride And Hydrochlorothiazide

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 Quinapril Hydrochloride; Hydrochlorothiazide.

Product ID0071-0223_1d3fab62-2114-4d5b-b07a-9b0f2b5a3efd
NDC0071-0223
Product TypeHuman Prescription Drug
Proprietary NameACCURETIC
Generic NameQuinapril Hydrochloride And Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1999-12-28
Marketing CategoryNDA / NDA
Application NumberNDA020125
Labeler NameParke-Davis Div of Pfizer Inc
Substance NameQUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Active Ingredient Strength20 mg/1; mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0071-0223-23

90 TABLET, FILM COATED in 1 BOTTLE (0071-0223-23)
Marketing Start Date1999-12-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0071-0223-23 [00071022323]

ACCURETIC TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020125
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1999-12-28

Drug Details

Active Ingredients

IngredientStrength
QUINAPRIL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:80e9d61d-9674-4ac4-b84c-79a875d408dd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 809858
  • 310796
  • 310797
  • 809854
  • 310809
  • 882559
    • UPC Code
  • 0300710223233
  • 0300710222236
  • 0300710220232

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    NDC Crossover Matching brand name "ACCURETIC" or generic name "Quinapril Hydrochloride And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0071-0220ACCURETICquinapril hydrochloride and hydrochlorothiazide
    0071-0222ACCURETICquinapril hydrochloride and hydrochlorothiazide
    0071-0223ACCURETICquinapril hydrochloride and hydrochlorothiazide
    0071-3112ACCURETICquinapril and hydrochlorothiazide
    0071-5212ACCURETICquinapril and hydrochlorothiazide
    31722-374Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    31722-375Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    31722-376Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    59762-0220quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    59762-0222quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    59762-0223quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    60505-3409Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    60505-3410Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    60505-3411Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide

    Trademark Results [ACCURETIC]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACCURETIC
    ACCURETIC
    75520049 2423789 Live/Registered
    WARNER-LAMBERT COMPANY LLC
    1998-07-16
    ACCURETIC
    ACCURETIC
    74088271 not registered Dead/Abandoned
    WARNER-LAMBERT COMPANY
    1990-08-15
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.