NDC11 00143916601
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 |
|---|---|
| 00143-9166-01 | 00143-9166 |
| 00143-9166-1 | 00143-9166 |
| 0143-9166-01 | 0143-9166 |
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 |
|---|---|---|---|---|---|---|
| XTRENBO | DENOSUMAB-QBDE | Hikma Pharmaceuticals USA Inc. | a48a3a33-6b0e-4cf4-8786-8f662d6ee77b | 2025-09-02 | Warnings, Adverse reactions | 0143-9166-01 0143-9166 00143916601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.