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Zestril (lisinopril)

Generic (originally Merck/AstraZeneca) · FDA-approved approved Small molecule Under review Quality 10/100

Zestril (generic name: lisinopril) is a Thiazide Diuretic [EPC] Small molecule drug developed by Generic (originally Merck/AstraZeneca). It is currently FDA-approved (first approved 1987) for Chronic heart failure, Hypertensive disorder, Myocardial infarction. Also known as: Zestril, Prinivil.

Inhibits angiotensin-converting enzyme (ACE), preventing conversion of angiotensin I to angiotensin II, lowering blood pressure and reducing cardiac workload.

Lisinopril is a small molecule that belongs to the class of angiotensin-converting enzyme (ACE) inhibitors, used to treat hypertension, heart failure, and heart attacks. It is typically taken orally and may take up to four weeks to achieve its full effect.

At a glance

Generic namelisinopril
Also known asZestril, Prinivil
SponsorGeneric (originally Merck/AstraZeneca)
Drug classThiazide Diuretic [EPC]
TargetAngiotensin-converting enzyme, Angiotensin-converting enzyme
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1987-12-29 (United States)

Mechanism of action

Lisinopril is a lysine analog of enalaprilat and the third ACE inhibitor approved in the US. Unlike most ACE inhibitors, it is not a prodrug and does not require hepatic activation, making it suitable for patients with liver disease. It is the most prescribed ACE inhibitor in the United States, with proven benefits in heart failure, post-MI, and diabetic nephropathy.

Approved indications

Boxed warnings

Common side effects

Serious adverse events

Key clinical trials

Patents

PatentExpiryType
96160962035-11-06Method of Use
100398002035-11-06Method of Use
104061992035-11-06Method of Use
124339312035-11-06Method of Use
102653702035-11-06Formulation
94631832035-11-06Formulation
111794342035-11-06Formulation
98147512035-11-06Formulation

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Zestril

What is Zestril?

Zestril (lisinopril) is a Thiazide Diuretic [EPC] drug developed by Generic (originally Merck/AstraZeneca), indicated for Chronic heart failure, Hypertensive disorder, Myocardial infarction.

How does Zestril work?

Inhibits angiotensin-converting enzyme (ACE), preventing conversion of angiotensin I to angiotensin II, lowering blood pressure and reducing cardiac workload.

What is Zestril used for?

Zestril is indicated for Chronic heart failure, Hypertensive disorder, Myocardial infarction, Superficial Ocular Infection.

Who makes Zestril?

Zestril is developed and marketed by Generic (originally Merck/AstraZeneca) (see full Generic (originally Merck/AstraZeneca) pipeline at /company/unknown).

What is the generic name of Zestril?

lisinopril is the generic (nonproprietary) name of Zestril.

Is Zestril also known as anything else?

Zestril is also known as Zestril, Prinivil.

What drug class is Zestril in?

Zestril belongs to the Thiazide Diuretic [EPC] class. See all Thiazide Diuretic [EPC] drugs at /class/thiazide-diuretic-epc.

When was Zestril approved?

Zestril was first approved on 1987-12-29 in United States.

What development phase is Zestril in?

Zestril is FDA-approved (marketed).

What are the side effects of Zestril?

Common side effects of Zestril include Hypotension, Headache, Dizziness, Cough, Chest pain, Hyperkalemia. Serious adverse events: Renal dysfunction, Pancreatitis, Stevens-Johnson syndrome, Toxic epidermal necrolysis.

What does Zestril target?

Zestril targets Angiotensin-converting enzyme, Angiotensin-converting enzyme and is a Thiazide Diuretic [EPC].

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing