NDC11 48878313004
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 |
|---|---|
| 48878-3130-04 | 48878-3130 |
| 48878-3130-4 | 48878-3130 |
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 |
|---|---|---|---|---|---|---|
| Clinpro 5000 | SODIUM FLUORIDE | Solventum US LLC | a20d3cf0-2e1f-4191-971e-9e47936b4580 | 2024-08-01 | Warnings, Adverse reactions | 48878-3130-4 48878-3130 48878313004 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.