NDC11 00173077602
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 |
|---|---|
| 00173-0776-02 | 00173-0776 |
| 00173-0776-2 | 00173-0776 |
| 00173-776-02 | 00173-776 |
| 0173-0776-02 | 0173-0776 |
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 |
|---|---|---|---|---|---|---|
| LAMICTAL | LAMOTRIGINE | GlaxoSmithKline LLC | d7e3572d-56fe-4727-2bb4-013ccca22678 | 2025-10-10 | Boxed warning, Warnings, Adverse reactions | 0173-0776-02 0173-0776 00173077602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.