NDC11 72789051330
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 |
|---|---|
| 72789-0513-30 | 72789-0513 |
| 72789-513-30 | 72789-513 |
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 |
|---|---|---|---|---|---|---|
| PredniSONE Tablets, USP, 10 mg | PREDNISONE | PD-Rx Pharmaceuticals, Inc. | bb32e309-e3c7-4009-bcd4-d97545b7e975 | 2026-06-04 | Warnings, Adverse reactions | 72789-513-30 72789-513 72789051330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.