Last reviewed · How we verify

GUANIDINE HYDROCHLORIDE

FDA-approved approved Small molecule Quality 5/100

Guanidine Hydrochloride is a marketed drug with a key composition patent expiring in 2028. The drug's market position and primary indication are not specified, but the patent expiry presents a significant competitive advantage by maintaining exclusivity until 2028. The primary risk is the potential for generic competition to enter the market immediately after the patent expires in 2028.

At a glance

Generic nameGUANIDINE HYDROCHLORIDE
ModalitySmall molecule
PhaseFDA-approved
First approval1939

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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