NDC11 00037024523
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 |
|---|---|
| 00037-0245-23 | 00037-0245 |
| 00037-245-23 | 00037-245 |
| 0037-0245-23 | 0037-0245 |
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 |
|---|---|---|---|---|---|---|
| DYMISTA | AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE | Viatris Specialty LLC | 4c557ec4-c4cf-11df-851a-0800200c9a66 | 2024-12-04 | Warnings, Adverse reactions | 0037-0245-23 0037-0245 00037024523 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.