NDC11 61755005051
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 |
|---|---|
| 61755-0050-51 | 61755-0050 |
| 61755-050-51 | 61755-050 |
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 |
|---|---|---|---|---|---|---|
| EYLEA HD | AFLIBERCEPT | Regeneron Pharmaceuticals, Inc | 86d8848b-111b-4da9-8957-7cccef1b8f66 | 2026-04-06 | Warnings, Adverse reactions | 61755-050-51 61755-050 61755005051 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.