NALFON (fenoprofen calcium) by Teva is analgesic, anti-inflammatory, and antipyretic properties. Approved for rheumatoid arthritis. First approved in 1976.
Drug data last refreshed 3h 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-mediated pain and inflammation. The drug provides analgesic, anti-inflammatory, and antipyretic effects through peripheral reduction of prostaglandin synthesis. It is administered orally in capsule form.
Minimal commercial activity with only 55 claims annually signals a shrinking product requiring defensive portfolio management rather than growth investment.
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 offers minimal career advancement; the product supports only sustaining/defensive roles on a declining franchise with shrinking headcount. Career progression would require lateral movement to growth products within Teva's portfolio rather than upward mobility within this brand.
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