NDC11 00173086910
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 |
|---|---|
| 00173-0869-10 | 00173-0869 |
| 00173-869-10 | 00173-869 |
| 0173-0869-10 | 0173-0869 |
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 |
|---|---|---|---|---|---|---|
| Anoro Ellipta | UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE | GlaxoSmithKline LLC | 2dbd0671-c565-40c5-bf0f-e324db26799c | 2023-06-02 | Warnings, Adverse reactions | 0173-0869-10 0173-0869 00173086910 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.