NDC11 72843044101
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 |
|---|---|
| 72843-0441-01 | 72843-0441 |
| 72843-0441-1 | 72843-0441 |
| 72843-441-01 | 72843-441 |
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 |
|---|---|---|---|---|---|---|
| Voriconazole | VORICONAZOLE | UBI Pharma Inc. | 9a81e485-7f26-45b6-bfd7-6114afb7def9 | 2025-06-20 | Warnings, Adverse reactions | 72843-441-01 72843-441 72843044101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.