NALFON (fenoprofen calcium) by Teva is analgesic, anti-inflammatory, and antipyretic properties. Approved for rheumatoid arthritis. First approved in 1976.
Drug data last refreshed 16h ago · AI intelligence enriched 1w ago
NALFON (fenoprofen calcium) is an oral NSAID approved in 1976 for rheumatoid arthritis that works by inhibiting cyclooxygenase (COX-1 and COX-2) to reduce prostaglandin synthesis. It provides analgesic, anti-inflammatory, and antipyretic effects by decreasing prostaglandin-mediated pain and inflammation in peripheral tissues.
With LOE approaching and only $23K in Part D spending, NALFON faces minimal commercial opportunity; expect a small, defensive brand team focused on maintaining existing patient populations 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.
NALFON presents minimal career growth opportunity, with zero linked jobs and a product in late decline approaching LOE. Roles focus on managed sunset, generic competition defense, and operational continuity rather than market expansion or innovation.
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