NDC11 00173071722
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 |
|---|---|
| 00173-0717-22 | 00173-0717 |
| 00173-717-22 | 00173-717 |
| 0173-0717-22 | 0173-0717 |
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 |
|---|---|---|---|---|---|---|
| ADVAIR HFA | FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE | GlaxoSmithKline LLC | dfaca6f9-3277-47b2-319d-1377917cb54c | 2024-05-23 | Warnings, Adverse reactions | 0173-0717-22 0173-0717 00173071722 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.