NDC11 81759000230
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 |
|---|---|
| 81759-0002-30 | 81759-0002 |
| 81759-002-30 | 81759-002 |
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 | BAMF Health Inc. | ef58c3cd-a922-c5fc-e053-2a95a90a9d74 | 2023-12-29 | Warnings, Adverse reactions | 81759-002-30 81759-002 81759000230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.