NDC11 72606002901
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 |
|---|---|
| 72606-0029-01 | 72606-0029 |
| 72606-0029-1 | 72606-0029 |
| 72606-029-01 | 72606-029 |
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 |
|---|---|---|---|---|---|---|
| STEQEYMA | USTEKINUMAB-STBA | CELLTRION USA, Inc. | 66085e17-e3f2-4196-8c81-87448e804b0c | 2026-04-07 | Warnings, Adverse reactions | 72606-029-01 72606-029 72606002901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.