NDC11 55513000304
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 |
|---|---|
| 55513-0003-04 | 55513-0003 |
| 55513-0003-4 | 55513-0003 |
| 55513-003-04 | 55513-003 |
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 |
|---|---|---|---|---|---|---|
| ARANESP | DARBEPOETIN ALFA | Amgen, Inc | 0fd36cb9-c4f6-4167-93c9-8530865db3f9 | 2026-07-07 | Boxed warning, Warnings, Adverse reactions | 55513-003-04 55513-003 55513000304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.