NDC 11014-0739 - 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: 11014-0739
Package NDCs from labels: 11014-0739-1
Manufacturer: Catalent Pharma Solutions, LLC | Hovione Farmaciência S.A. | Catalent CTS, LLC
Effective date: 2025-11-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Voydeya 50mg Tablets	Catalent Pharma Solutions, LLC \| Hovione Farmaciência S.A. \| Catalent CTS, LLC	2025-11-27	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11014-0739-1	Voydeya	90 in 1 BOTTLE	TABLET, FILM COATED	90		2
11014-0739-1	Voydeya	1 in 1 CARTON	TABLET, FILM COATED	1		2

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 · 2 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 rxcui: 2678957 rxcui: 2678963 unii: JM8C1SFX0U
4492340f-772e-b5ce-e063-6394a90affa3			437a17ba-6ef6-1a7b-e063-6394a90a6565	2025-11-27		Exact identifier spl id: 4492340f-772e-b5ce-e063-6394a90affa3 spl set id: 437a17ba-6ef6-1a7b-e063-6394a90a6565

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.