NDC11 00143916501
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 |
|---|---|
| 00143-9165-01 | 00143-9165 |
| 00143-9165-1 | 00143-9165 |
| 0143-9165-01 | 0143-9165 |
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 |
|---|---|---|---|---|---|---|
| ENOBY | DENOSUMAB-QBDE | Hikma Pharmaceuticals USA Inc. | 815d3ba4-27a1-4a06-925a-a87f35442bdb | 2026-01-16 | Boxed warning, Warnings, Adverse reactions | 0143-9165-01 0143-9165 00143916501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.