NDC11 47335070708
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 |
|---|---|
| 47335-0707-08 | 47335-0707 |
| 47335-0707-8 | 47335-0707 |
| 47335-707-08 | 47335-707 |
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 |
|---|---|---|---|---|---|---|
| Topiramate | TOPIRAMATE | Sun Pharmaceutical Industries, Inc. | 3c909a53-ae66-4b28-a741-b60bb25a69cf | 2026-06-01 | Warnings, Adverse reactions | 47335-707-08 47335-707 47335070708 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.