NDC 25682-043-90 - 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: 25682-043
Requested NDC: 25682-043-90
Package NDCs from labels: 25682-043-92, 25682-043-90
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
Label	Manufacturer	Effective date	Type
Voydeya - Alexion Pharmaceuticals Inc.	Alexion Pharmaceuticals Inc.	2026-05-12	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
25682-043-90	Voydeya	90 in 1 BOTTLE	TABLET, FILM COATED	90	100 mg	5
25682-043-92	Voydeya	90 in 1 BOTTLE	TABLET, FILM COATED	90		5
25682-043-92	Voydeya	2 in 1 CARTON	TABLET, FILM COATED	2		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
25682-043	VOYDEYA (DANICOPAN) TABLET, FILM COATED VOYDEYA (DANICOPAN) KIT [ALEXION PHARMACEUTICALS INC.]	3	Current NDC, 2 package rows	20241210_ab8d1cbd-a28b-4d49-82ab-5c7460719ac7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
25682-043-92	EA - Each	25682-043	b013ed28-f19d-4d2e-9ff7-2654d27509f0	1	2024-05-16

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Voydeya	DANICOPAN	Alexion Pharmaceuticals Inc.	ab8d1cbd-a28b-4d49-82ab-5c7460719ac7	2026-05-12	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: NDA218037 ndc (package): 25682-046-92 ndc (package): 25682-040-90 ndc (package): 25682-043-90 ndc (package): 25682-043-92 ndc (product): 25682-043 ndc (product): 25682-046 ndc11 (package): 25682004390 rxcui: 2678957 rxcui: 2678965 rxcui: 2678967 rxcui: 2678974 rxcui: 2678973 rxcui: 2678963 rxcui: 2678972 rxcui: 2678975 spl id: cd0113b0-d5d6-4b03-9f6f-4d80bdcb71fe spl set id: ab8d1cbd-a28b-4d49-82ab-5c7460719ac7 unii: JM8C1SFX0U