NDC11 24562000230
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 |
|---|---|
| 24562-0002-30 | 24562-0002 |
| 24562-002-30 | 24562-002 |
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 |
|---|---|---|---|---|---|---|
| Sodium Fluoride F 18 | SODIUM FLUORIDE F-18 | Biomedical Research Foundation of Northwest Louisiana | 4c45fe05-e3b7-4383-966c-4e218ff6f94a | 2026-06-10 | Warnings, Adverse reactions | 24562-002-30 24562-002 24562000230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.