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Sold as Inqovi. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 1 application for Cedazuridine; Decitabine (sold as Inqovi), first approved Jul 7, 2020, with 1 new use approved and 0 published complete response letters.
First approved: Jul 7, 2020
Applications: 1
New uses approved: 1
Complete response letters: 0
First approved in the EU: Sep 15, 2023
Approvals in the EU (EMA)
First approved in the EU 38 months after the US. Centrally authorised medicines, matched by ingredient; see all EU approvals
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
