LICART (diclofenac epolamine) by IBSA Institut Biochimique is analgesic, anti-inflammatory, and antipyretic properties. First approved in 2018.
Drug data last refreshed 13h ago · AI intelligence enriched 1w ago
LICART is a topical transdermal diclofenac epolamine system approved in 2018 for localized pain and inflammation. It is a nonsteroidal anti-inflammatory drug (NSAID) that works by inhibiting cyclooxygenase (COX-1 and COX-2) enzymes to reduce prostaglandin synthesis. The formulation includes heparin sodium and demonstrates no systemic anticoagulant effects at therapeutic doses.
LICART is in peak commercial lifecycle with modest Part D uptake ($9M, 8,871 claims in 2023), indicating stable demand but limited market penetration or team expansion opportunity.
analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of diclofenac, like that of other NSAIDs, is not completely understood but involves inhibition of cyclooxygenase (COX-1 and COX-2). Diclofenac is a potent inhibitor of prostaglandin synthesis in vitro. Diclofenac…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Study of PK and Safety of the LicartTM Topical System in Pediatric and Adult Participants with Minor Soft Tissue Injury
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
LICART currently shows zero linked job openings, reflecting its niche positioning and modest market scale. Working on this product offers exposure to topical NSAID commercialization and market access strategy, but limited team growth or advancement opportunities given peak-stage lifecycle and small sales footprint.
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