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Oxynorm via PCA

Helsinki University Central Hospital · FDA-approved active Small molecule Quality 2/100

Oxynorm via PCA is a Small molecule drug developed by Helsinki University Central Hospital. It is currently FDA-approved.

Oxynorm, administered via patient-controlled analgesia (PCA), is a marketed product by Helsinki University Central Hospital. The key composition patent for Oxynorm is set to expire in 2028, providing a clear timeline for potential generic competition. The primary risk is the loss of exclusivity post-2028, which could significantly impact revenue.

At a glance

Generic nameOxynorm via PCA
SponsorHelsinki University Central Hospital
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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Frequently asked questions about Oxynorm via PCA

What is Oxynorm via PCA?

Oxynorm via PCA is a Small molecule drug developed by Helsinki University Central Hospital.

Who makes Oxynorm via PCA?

Oxynorm via PCA is developed and marketed by Helsinki University Central Hospital (see full Helsinki University Central Hospital pipeline at /company/helsinki-university-central-hospital).

What development phase is Oxynorm via PCA in?

Oxynorm via PCA is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing