NDC11 71205036206
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 |
|---|---|
| 71205-0362-06 | 71205-0362 |
| 71205-0362-6 | 71205-0362 |
| 71205-362-06 | 71205-362 |
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 | Proficient Rx LP | 94f8ec56-667e-4eda-832d-f2936f12dc36 | 2024-05-01 | Warnings, Adverse reactions | 71205-362-06 71205-362 71205036206 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.