FDA.reportPublic FDA data

NDC 72493-104 - ZUSDURI

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
72493-104
Package NDCs from labels
72493-104-40
Manufacturer
UroGen Pharma, Inc | UroGen Pharma, Ltd.
Effective date
2025-06-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ZUSDURI - UroGen Pharma, Inc | UroGen Pharma, Ltd.UroGen Pharma, Inc | UroGen Pharma, Ltd.2025-06-20HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72493-104-40ZUSDURI1 in 1 VIAL, SINGLE-DOSEPOWDER, FOR SOLUTION240 mg2