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Sold as Ansaid. Every FDA application for this active ingredient: 1 branded and 8 generic.
As of Nov 13, 2026, FDA lists 9 applications for Flurbiprofen (sold as Ansaid), first approved Oct 31, 1988, with 0 new uses approved and 0 published complete response letters.
First approved: Oct 31, 1988
Applications: 9
New uses approved: 0
Complete response letters: 0
Medicare spending, 2025: $1.5M
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
Flurbiprofen
Part D
$840K
+33%
4,271
Flurbiprofen Sodium
Part D
$637K
-4%
8,271
Lurbiro
Part D
$0K
New
0
Clinical Trials
20 open or ongoing studies name this ingredient as an intervention, including as a comparator; newest first. See all
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA
Teva
Sun Pharm Inds Inc