NDC11 55513050902
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 |
|---|---|
| 55513-0509-02 | 55513-0509 |
| 55513-0509-2 | 55513-0509 |
| 55513-509-02 | 55513-509 |
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 |
|---|---|---|---|---|---|---|
| Evenity | ROMOSOZUMAB-AQQG | Amgen, Inc | 471baba2-7154-4488-9891-0db2f46791e7 | 2026-07-16 | Boxed warning, Warnings, Adverse reactions | 55513-509-02 55513-509 55513050902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.