NDC11 62756056983
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 |
|---|---|
| 62756-0569-83 | 62756-0569 |
| 62756-569-83 | 62756-569 |
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 |
|---|---|---|---|---|---|---|
| deferasirox | DEFERASIROX | Sun Pharmaceutical Industries, Inc. | 4a2e1bd2-9f3a-40ec-94a2-bc76350d6d4b | 2023-12-26 | Boxed warning, Warnings, Adverse reactions | 62756-569-83 62756-569 62756056983 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.