NDC11 43498010115
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 |
|---|---|
| 43498-0101-15 | 43498-0101 |
| 43498-101-15 | 43498-101 |
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 |
|---|---|---|---|---|---|---|
| Burkhart | SODIUM FLUORIDE | Burkhart Dental Supply Inc | 87b3b8b8-780f-492d-bd75-b005edd55baa | 2022-02-02 | Warnings | 43498-101-15 43498-101 43498010115 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.