NALFON (fenoprofen calcium) by Teva is analgesic, anti-inflammatory, and antipyretic properties. Approved for rheumatoid arthritis. First approved in 1976.
Drug data last refreshed 1h ago · AI intelligence enriched 3w ago
NALFON (fenoprofen calcium) is an oral NSAID that inhibits cyclooxygenase (COX-1 and COX-2) to reduce prostaglandin synthesis, providing analgesic, anti-inflammatory, and antipyretic effects. It is indicated for rheumatoid arthritis and works by decreasing prostaglandins in peripheral tissues to reduce inflammation and pain. The drug has been on the market since 1976 and is now approaching loss of exclusivity.
As a mature product approaching loss of exclusivity with minimal spending ($23K in Part D claims), the NALFON brand team is likely small and focused on defending share against generic and competitive erosion rather than growth.
analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of FENOPROFEN CALCIUM, like that of other NSAIDs, is not completely understood but involves inhibition of cyclooxygenase (COX-1 and COX-2). Fenoprofen is a potent inhibitor of prostaglandin synthesis in vitro.…
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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.
Working on NALFON in a LOE-approaching environment means your role will focus on defending market share, managing generic transition, and optimizing pricing and reimbursement rather than growth. Career advancement may be limited due to the product's mature stage and modest commercial investment ($23K in Part D spending, 55 claims).
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