NDC11 00245107230
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 |
|---|---|
| 00245-1072-30 | 00245-1072 |
| 0245-1072-30 | 0245-1072 |
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 |
|---|---|---|---|---|---|---|
| QUDEXY XR | TOPIRAMATE | Upsher-Smith Laboratories, LLC | 46f54677-3a22-4c38-9b92-923020164e15 | 2026-09-03 | Warnings, Adverse reactions | 0245-1072-30 0245-1072 00245107230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.