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Intranasal Fentanyl

Columbia University · FDA-approved active Small molecule Quality 5/100

Intranasal Fentanyl, marketed by Columbia University, holds a position in the pain management segment with a key composition patent expiring in 2028. The drug's primary strength lies in its rapid onset of action, making it a preferred option for acute pain relief. The primary risk is the intense competition in the pain management market, which could impact its market share and revenue.

At a glance

Generic nameIntranasal Fentanyl
Also known asFentanyl, Instanyl
SponsorColumbia University
ModalitySmall molecule
PhaseFDA-approved

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
ClinicalTrials.govTrial enrolment, design, endpoints, results