NDC11 59448010000
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 |
|---|---|
| 59448-0100-0 | 59448-0100 |
| 59448-0100-00 | 59448-0100 |
| 59448-100-00 | 59448-100 |
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 |
|---|---|---|---|---|---|---|
| NewYork-Presbyterian Amenity | SODIUM MONOFLUOROPHOSPATE | ASP Global, LLc | 4b307471-445d-4c51-a499-d074a8172f20 | 2024-12-17 | Warnings | 59448-100-00 59448-100 59448010000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.