REZUROCK (BELUMOSUDIL)
Summary
FDA approved REZUROCK (BELUMOSUDIL) by KADMON PHARMS LLC. NDA (New Drug) approval (Labeling) on 2026-01-15. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA214783-12
Action Date
2026-01-15
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
REZUROCK (generic: BELUMOSUDIL), TABLET, ORAL. Application: NDA214783
Company
Context & Analysis
Frequently Asked Questions
How often does KADMON PHARMS LLC have FDA actions?
This is the only FDA action we have on record for KADMON PHARMS LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA214783-12" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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