NDC11 49502080632
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 |
|---|---|
| 49502-0806-32 | 49502-0806 |
| 49502-806-32 | 49502-806 |
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 |
|---|---|---|---|---|---|---|
| YUPELRI | REVEFENACIN | Viatris Specialty LLC | 6dfebf04-7c90-436a-9b16-750d3c1ee0a6 | 2022-05-03 | Warnings, Adverse reactions | 49502-806-32 49502-806 49502080632 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.