NDC11 00173091261
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 |
|---|---|
| 00173-0912-61 | 00173-0912 |
| 00173-912-61 | 00173-912 |
| 0173-0912-61 | 0173-0912 |
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 |
|---|---|---|---|---|---|---|
| ZEJULA | NIRAPARIB | GlaxoSmithKline LLC | b7f675e2-159c-490c-b6f4-3f16d9492b7d | 2026-07-28 | Warnings, Adverse reactions | 0173-0912-61 0173-0912 00173091261 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.