NDC11 47335017795
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 |
|---|---|
| 47335-0177-95 | 47335-0177 |
| 47335-177-95 | 47335-177 |
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 |
|---|---|---|---|---|---|---|
| ILUMYA | TILDRAKIZUMAB-ASMN | Sun Pharmaceutical Industries, Inc. | c6a322bb-51b9-4f0e-8642-62a9682ffcde | 2026-07-29 | Warnings, Adverse reactions | 47335-177-95 47335-177 47335017795 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.