NDC11 72789017801
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 |
|---|---|
| 72789-0178-01 | 72789-0178 |
| 72789-0178-1 | 72789-0178 |
| 72789-178-01 | 72789-178 |
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 |
|---|---|---|---|---|---|---|
| Primidone | PRIMIDONE | PD-Rx Pharmaceuticals, Inc. | 6046e4e9-0c1e-4d1f-85fa-d2ce25c5dc34 | 2025-10-20 | Warnings, Adverse reactions | 72789-178-01 72789-178 72789017801 |
| Primidone | PRIMIDONE | PD-Rx Pharmaceuticals, Inc. | 0193c0a4-f593-609c-e063-6294a90aaa68 | 2025-06-10 | Warnings, Adverse reactions | 72789-178 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.