NDC11 80491801203
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 80491-8012-03 | 80491-8012 |
| 80491-8012-3 | 80491-8012 |
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 |
|---|---|---|---|---|---|---|
| TRYVIO | APROCITENTAN | Idorsia Pharmaceuticals Ltd | dfe7a2ee-612c-4aba-834a-d68e6b59a0a6 | 2026-08-14 | Boxed warning, Warnings, Adverse reactions | 80491-8012-3 80491-8012 80491801203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.