GRAFAPEX (TREOSULFAN)
Summary
FDA approved GRAFAPEX (TREOSULFAN) by MEDEXUS. NDA (New Drug) approval (Labeling) on 2025-02-05. POWDER, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA214759-1
Action Date
2025-02-05
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
GRAFAPEX (generic: TREOSULFAN), POWDER, INTRAVENOUS. Application: NDA214759
Company
Context & Analysis
Frequently Asked Questions
How often does MEDEXUS have FDA actions?
This is the only FDA action we have on record for MEDEXUS in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA214759-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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