Last reviewed · How we verify

TERAZOSIN HYDROCHLORIDE

FDA-approved approved Small molecule Quality 20/100

Terazosin Hydrochloride is a marketed drug primarily indicated for symptomatic Benign Prostatic Hyperplasia (BPH). Its key strength lies in its established market presence and the key composition patent, which is set to expire in 2028. The primary risk is the potential increase in competition following the patent expiry.

At a glance

Generic nameTERAZOSIN HYDROCHLORIDE
ModalitySmall molecule
PhaseFDA-approved
First approval1987

Approved indications

Common side effects

Serious adverse events

Key clinical trials

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

Competitive intelligence

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