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H-Bupivacaine

Pontificia Universidad Catolica de Chile · FDA-approved active Small molecule Quality 2/100

H-Bupivacaine is a Small molecule drug developed by Pontificia Universidad Catolica de Chile. It is currently FDA-approved. Also known as: Hyperbaric bupivacaine.

H-Bupivacaine, marketed by Pontificia Universidad Catolica de Chile, is an established product in the local anesthetic market. The key composition patent is set to expire in 2028, providing a clear period of exclusivity and potential revenue stability. The primary risk lies in the lack of disclosed primary trial results and competitors, which may impact market confidence and positioning.

At a glance

Generic nameH-Bupivacaine
Also known asHyperbaric bupivacaine
SponsorPontificia Universidad Catolica de Chile
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 H-Bupivacaine

What is H-Bupivacaine?

H-Bupivacaine is a Small molecule drug developed by Pontificia Universidad Catolica de Chile.

Who makes H-Bupivacaine?

H-Bupivacaine is developed and marketed by Pontificia Universidad Catolica de Chile (see full Pontificia Universidad Catolica de Chile pipeline at /company/pontificia-universidad-catolica-de-chile).

Is H-Bupivacaine also known as anything else?

H-Bupivacaine is also known as Hyperbaric bupivacaine.

What development phase is H-Bupivacaine in?

H-Bupivacaine is FDA-approved (marketed).

Related

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