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Sold as Emend, Fosaprepitant Dimeglumine, Focinvez, Navitrux. Every FDA application for this active ingredient: 4 branded and 19 generic.
As of Nov 15, 2026, FDA lists 23 applications for Fosaprepitant Dimeglumine (sold as Emend, Fosaprepitant Dimeglumine, Focinvez and others), first approved Jan 25, 2008, with 4 new uses approved and 1 published complete response letter.
First approved: Jan 25, 2008
Applications: 23
New uses approved: 4
Complete response letters: 1
Medicare spending, 2025: $16.3M
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
FOCINVEZ
Part B
$13.5M
New
6,684
Emend
Part B
$1.5M
-32%
18,001
Fosaprepitant Dimeglumine
Part D
$609K
+17%
931
Fosaprepitant Dimeglumine
Part B
$567K
+106%
1,032
Focinvez
Part D
$60K
New
22
What Pharmacies Pay
Median price per unit across package codes in CMS's weekly NADAC survey, Nov 11, 2026, before rebates; see every drug's price change
EMEND 125 MG POWDER PACKET: $327.38 per unitBrand · +0% in a year
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