NDC11 10122010401
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 |
|---|---|
| 10122-0104-01 | 10122-0104 |
| 10122-0104-1 | 10122-0104 |
| 10122-104-01 | 10122-104 |
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 |
|---|---|---|---|---|---|---|
| FERRIPROX | DEFERIPRONE | Chiesi USA, Inc. | 946718ff-df43-1baa-74d1-e5bcfbe8ad86 | 2026-01-28 | Boxed warning, Warnings, Adverse reactions | 10122-104-01 10122-104 10122010401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.