NDC11 52817086008
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 |
|---|---|
| 52817-0860-08 | 52817-0860 |
| 52817-0860-8 | 52817-0860 |
| 52817-860-08 | 52817-860 |
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 |
|---|---|---|---|---|---|---|
| Prednisolone | PREDNISOLONE ORAL | TRUPHARMA, LLC | 4f83514d-5342-4748-a0d3-b0306ca303c8 | 2026-09-02 | Warnings, Adverse reactions | 52817-860-08 52817-860 52817086008 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.