NDC11 48878406103
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 |
|---|---|
| 48878-4061-03 | 48878-4061 |
| 48878-4061-3 | 48878-4061 |
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 |
|---|---|---|---|---|---|---|
| OMNI | STANNOUS FLUORIDE | Solventum US LLC | 0c2a81b1-65b5-432b-8e66-30432a245aba | 2024-08-01 | Warnings | 48878-4061-3 48878-4061 48878406103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.