NDC11 63323059930
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 |
|---|---|
| 63323-0599-30 | 63323-0599 |
| 63323-599-30 | 63323-599 |
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 |
|---|---|---|---|---|---|---|
| Deferoxamine | DEFEROXAMINE MESYLATE | Fresenius Kabi USA, LLC | d91e16df-8daa-4cd2-86a2-273eaa2446e0 | 2026-06-15 | Warnings, Adverse reactions | 63323-599-30 63323-599 63323059930 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.