NDC 25682-040 - Voydeya

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
25682-040
Package NDCs from labels
25682-040-90
Manufacturer
Alexion Pharmaceuticals Inc.
Effective date
2026-05-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Voydeya - Alexion Pharmaceuticals Inc.Alexion Pharmaceuticals Inc.2026-05-12HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
25682-040-90Voydeya90 in 1 BOTTLETABLET, FILM COATED9050 mg5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25682-040VOYDEYA (DANICOPAN) TABLET, FILM COATED VOYDEYA (DANICOPAN) KIT [ALEXION PHARMACEUTICALS INC.]3Unmatched20241210_ab8d1cbd-a28b-4d49-82ab-5c7460719ac7.zip