NDC11 73555050000
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 |
|---|---|
| 73555-0500-0 | 73555-0500 |
| 73555-0500-00 | 73555-0500 |
| 73555-500-00 | 73555-500 |
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 |
|---|---|---|---|---|---|---|
| Revuforj | REVUMENIB | Syndax Pharmaceuticals, Inc. | 6eb3cdbc-0e74-477d-82d6-3bb172d3f63f | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 73555-500-00 73555-500 73555050000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.