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EMLA

University of Colorado, Denver · FDA-approved active Small molecule Quality 6/100

EMLA, marketed by the University of Colorado, Denver, is a topical anesthetic with a key composition patent expiring in 2028. Despite the unknown mechanism of action, EMLA holds a unique position in the market due to its established presence and lack of direct competitors. The primary risk is the potential for generic entry following the 2028 patent expiry, which could erode market share and revenue.

At a glance

Generic nameEMLA
Also known asEMLA Cream, lidocaine 25 mg/g + prilocaine 25 mg/g cream, EMLA 5% cream, EMLA cream, a topical analgesic, will be applied prior to the procedure, EMLA®, AstraZeneca, Cotia, SP, Brazil
SponsorUniversity of Colorado, Denver
ModalitySmall molecule
Therapeutic areaOther
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

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