NDC11 82667001805
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 |
|---|---|
| 82667-0018-05 | 82667-0018 |
| 82667-0018-5 | 82667-0018 |
| 82667-018-05 | 82667-018 |
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 |
|---|---|---|---|---|---|---|
| Byooviz | RANIBIZUMAB-NUNA | Harrow Eye, LLC | 77b53b2c-da0e-44b2-ade4-b08ff75a7584 | 2025-11-26 | Warnings, Adverse reactions | 82667-018-05 82667-018 82667001805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.