NDC11 00131248035
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 |
|---|---|
| 00131-2480-35 | 00131-2480 |
| 0131-2480-35 | 0131-2480 |
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 |
|---|---|---|---|---|---|---|
| Vimpat | LACOSAMIDE | UCB, Inc. | 9e79b42c-38a3-4b2c-a196-a5a1948250e2 | 2026-05-12 | Warnings, Adverse reactions | 0131-2480-35 0131-2480 00131248035 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.