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Selegiline Transdermal System

Somerset Pharmaceuticals · FDA-approved active Small molecule Quality 5/100

Selegiline Transdermal System, marketed by Somerset Pharmaceuticals, holds a position in the therapeutic landscape for its indicated use, though specific details on its primary indication and revenue are not provided. A key strength of the product is its unique transdermal delivery mechanism, which may offer a competitive edge over oral formulations. The primary risk to consider is the key composition patent expiry in 2028, which could lead to increased competition from generic alternatives.

At a glance

Generic nameSelegiline Transdermal System
Also known asEMSAM
SponsorSomerset Pharmaceuticals
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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