NDC11 51672413306
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 |
|---|---|
| 51672-4133-06 | 51672-4133 |
| 51672-4133-6 | 51672-4133 |
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 |
|---|---|---|---|---|---|---|
| Lamotrigine | LAMOTRIGINE | Sun Pharmaceutical Industries, Inc. | b829f9b2-f0ac-408a-a6f4-18b72150227d | 2026-06-03 | Boxed warning, Warnings, Adverse reactions | 51672-4133-6 51672-4133 51672413306 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.