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PSEUDOEPHEDRINE SULFATE

FDA-approved approved Small molecule Quality 20/100

Pseudoephedrine sulfate is a marketed drug primarily indicated for the relief of hay fever symptoms. Its key strength lies in its well-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 namePSEUDOEPHEDRINE SULFATE
ModalitySmall molecule
PhaseFDA-approved
First approval1963

Approved indications

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