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Zusduri FDA Approval History

Last updated by Judith Stewart, BPharm on June 13, 2025.

FDA Approved: Yes (First approved June 12, 2025)
Brand name: Zusduri
Generic name: mitomycin
Dosage form: for Intravesical Solution
Previous Name: UGN-102
Company: UroGen Pharma Ltd.
Treatment for: Bladder Cancer

Zusduri (mitomycin) is a sustained release, hydrogel-based formulation of mitomycin for intravesical treatment of low-grade intermediate-risk non-muscle invasive bladder cancer (LG-IR-NMIBC).

Development timeline for Zusduri

DateArticle
Jun 12, 2025Approval FDA Approves Zusduri (mitomycin) for Recurrent Low-Grade Intermediate-Risk Non-Muscle Invasive Bladder Cancer
Oct 15, 2024UroGen Announces FDA Acceptance of its New Drug Application for UGN-102
Aug 14, 2024UroGen Submits Completed UGN-102 NDA Seeking Approval as the First FDA-Approved Treatment for Low-Grade Intermediate-Risk Non-Muscle Invasive Bladder Cancer
Jan 24, 2024UroGen Initiates Submission of a Rolling NDA to the FDA for UGN-102
Oct  3, 2023Following Pre-NDA Meeting with the FDA, UroGen Announces Rolling NDA Submission for UGN-102 to Begin January 2024

Further information

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