NDC11 59651048705
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 |
|---|---|
| 59651-0487-05 | 59651-0487 |
| 59651-0487-5 | 59651-0487 |
| 59651-487-05 | 59651-487 |
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 | PREDNISONE | Aurobindo Pharma Limited | b1ac4c92-e1fd-4015-b172-0932790ae019 | 2024-02-16 | Warnings, Adverse reactions | 59651-487-05 59651-487 59651048705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.