NDC11 80425051002
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 |
|---|---|
| 80425-0510-02 | 80425-0510 |
| 80425-0510-2 | 80425-0510 |
| 80425-510-02 | 80425-510 |
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 |
|---|---|---|---|---|---|---|
| Lacosamide | LACOSAMIDE | Advanced Rx of Tennessee, LLC | 325df1b7-4908-0c03-e063-6294a90ad844 | 2025-04-09 | Warnings, Adverse reactions | 80425-0510-2 80425-0510 80425051002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.