FDA.reportPublic FDA data

NDC 74725-101 - ILLUCCIX

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
74725-101
Package NDCs from labels
74725-101-25
Manufacturer
Telix Pharmaceuticals (US) Inc. | Telix Innovations
Effective date
2025-12-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ILLUCCIX - Telix Pharmaceuticals (US) Inc. | Telix InnovationsTelix Pharmaceuticals (US) Inc. | Telix Innovations2025-12-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74725-101-25ILLUCCIX1 in 1 VIAL, MULTI-DOSEINJECTION, POWDER, LYOPHILIZED,125 ug15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74725-101ILLUCCIX (KIT FOR THE PREPARATION OF GALLIUM GA 68 GOZETOTIDE INJECTION) KIT [TELIX PHARMACEUTICALS (US) INC.]9Unmatched20241010_d4643b31-9b4f-673f-e053-2a95a90a559d.zip