Registered Malawi · PMRA

ACCUPRIL-20 20MG TABLET

QUINAPRIL HYDROCHLORIDE

PMPB/PL135/6 TABLET INN generic

What it does

Quinapril is a type of medication known as an ACE inhibitor, used to help lower blood pressure.

Commonly used for: high blood pressure (hypertension), heart failure

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
PMPB/PL135/6
Registration date
14/08/2001
Expiry date
30/06/2007
Status
Registered
Active ingredient
QUINAPRIL HYDROCHLORIDE
Dosage form
TABLET
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
-
Applicant / LTR
-
Country of origin
-

Source: Pharmacy and Medicines Regulatory Authority · fetched 2026-04-21 17:37:38 · updated 2026-09-19 04:30:22

Disclaimer: This information is sourced from Pharmacy and Medicines Regulatory Authority (Malawi). Always consult a qualified healthcare professional before using any medication.

About this medicine

Quinapril is a type of medication known as an ACE inhibitor, used to help lower blood pressure.

What it treats

  • high blood pressure (hypertension)
  • heart failure

How it works

Quinapril works by relaxing blood vessels, making it easier for the heart to pump blood and lowering blood pressure.

Who it's for

Quinapril is for adults who need help managing their blood pressure or treating heart failure.

Drug class

ACE inhibitors

Cautions

  • • Be careful if you're taking medications that can cause a sudden drop in blood pressure.
  • • Avoid medications that lower blood pressure.
  • • Be cautious with drugs that can raise potassium levels in the blood.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Quinapril

BNF-referenced

Quinapril is an angiotensin converting enzyme (ACE) inhibitor used primarily for the treatment of hypertension and as an adjunct in heart failure management. As a prodrug, Quinapril is converted to its active form, Quinaprilat, which exerts its effects by inhibiting the conversion of angiotensin I to angiotensin II, thereby reducing vasoconstriction and blood pressure. It also has a favorable pharmacokinetic profile that allows for once-daily dosing.

Indications

  • Essential hypertension
  • Heart failure (adjunct treatment)

Dosage

Children: Refer to the BNF for Children for specific

Adults: Initially 2 mg once daily for at least 2 weeks, then increased if tolerated to 4 mg once daily. The maximum dose is 40 mg per day, adjusted according to response. For heart failure, the initial dose is 2.5 mg once daily, which can be increased if tolerated.

Mechanism of action

Quinaprilat prevents the conversion of angiotensin I to angiotensin II by inhibiting angiotensin converting enzyme. This results in decreased angiotensin II levels, leading to vasodilation, reduced vascular resistance, and decreased blood pressure. Additionally, it reduces the breakdown of bradykinin, which has vasodilatory effects. Lower levels of angiotensin II also decrease the production of plasminogen activator inhibitor-1 (PAI-1), thereby reducing the risk of thrombosis, particularly following myocardial infarction.

Pharmacodynamics

Quinapril is a prodrug that converts to Quinaprilat, an effective ACE inhibitor. It has a wide therapeutic window and long duration of action, making it suitable for once-daily administration. It effectively lowers blood pressure and provides symptomatic relief in heart failure by reducing preload and afterload on the heart.

Pharmacokinetics

Quinapril is absorbed after oral administration, with peak plasma concentrations typically occurring within 1 hour. It has a half-life of approximately 2 hours, but its active metabolite, Quinaprilat, has a longer half-life of about 9 hours. The drug is primarily excreted via the kidneys, necessitating dose adjustments in patients with renal impairment. Food does not significantly affect the absorption of Quinapril.

Adverse effects

  • Muscle cramps
  • Visual disturbances
  • Hypoglycaemia
  • Malaise
  • Mood alterations
  • Cholestasis

Interactions

  • ACE inhibitors

Precautions

  • Caution in renal impairment
  • Caution in elderly patients

Pregnancy

Not recommended; caution should be exercised in women who are pregnant or planning to become pregnant.

Breast-feeding

Not recommended; alternative treatment options with better established safety during breastfeeding are available.

Storage

Store in a cool, dry place away from direct sunlight.

Formulations

  • Quinapril 2.5 mg tablets
  • Quinapril 5 mg tablets
  • Quinapril 10 mg tablets
  • Quinapril 20 mg tablets
BNF 85 (British National Formulary) p.208 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: Quinapril

PubChem CID 54892

Molecular formula: C25H30N2O5

Mechanism of action

Angiotensin II constricts coronary blood vessels and is positively inotropic, which under normal circumstances, would increase vascular resistance and oxygen consumption. This action can eventually lead to myocyte hypertrophy and vascular smooth muscle cell proliferation. Angiotensin II also stimulates production of plasminogen activator inhibitor-1 (PAI-1), increasing the risk of thrombosis. Quinaprilat prevents the conversion of angiotensin I to angiotensin II by inhibition of angiotensin converting enzyme, and also reduces the breakdown of bradykinin. Reduced levels of angiotensin II lead to lower levels of PAI-1, reducing the risk of thrombosis, especially after a myocardial infarction.

Pharmacodynamics

Quinapril is a prodrug of an angiotensin converting enzyme (ACE) inhibitor used in the treatment of hypertension or adjunct in the treatment of heart failure. Quinapril has a wide therapeutic window and a long duration of action as it is given in doses of 10-80mg once daily.

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

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