NDC11 80425041801
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 |
|---|---|
| 80425-0418-01 | 80425-0418 |
| 80425-0418-1 | 80425-0418 |
| 80425-418-01 | 80425-418 |
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 |
|---|---|---|---|---|---|---|
| Desonide | DESONIDE | Advanced Rx of Tennessee, LLC | 1d7632a7-0f27-9e5d-e063-6294a90ad21f | 2024-07-17 | Adverse reactions | 80425-0418-1 80425-0418 80425041801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.