NDC 11014-0739-1 - 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
- Requested NDC
- 11014-0739-1
- 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 | 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 | 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.
| 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 | 2678957 2678963 JM8C1SFX0U |
| 4492340f-772e-b5ce-e063-6394a90affa3 | 437a17ba-6ef6-1a7b-e063-6394a90a6565 | 2025-11-27 | 4492340f-772e-b5ce-e063-6394a90affa3 437a17ba-6ef6-1a7b-e063-6394a90a6565 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.