NDC11 73289006502
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 |
|---|---|
| 73289-0065-02 | 73289-0065 |
| 73289-0065-2 | 73289-0065 |
| 73289-065-02 | 73289-065 |
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 |
|---|---|---|---|---|---|---|
| MOTPOLY XR | LACOSAMIDE | Aucta Pharmaceuticals, Inc. | fb8235b4-4cd3-6f22-e053-6294a90a545c | 2025-07-16 | Warnings, Adverse reactions | 73289-0065-2 73289-0065 73289006502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.