NDC11 65219053010
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 |
|---|---|
| 65219-0530-10 | 65219-0530 |
| 65219-530-10 | 65219-530 |
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 |
|---|---|---|---|---|---|---|
| Manganese | MANGANESE | Fresenius Kabi USA, LLC | 6feb30f0-8b6e-4729-8618-907baf29a2c7 | 2025-11-18 | Warnings, Adverse reactions | 65219-530-10 65219-530 65219053010 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.