NDC11 48783050040
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 |
|---|---|
| 48783-0500-40 | 48783-0500 |
| 48783-500-40 | 48783-500 |
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 |
|---|---|---|---|---|---|---|
| Enamelon Preventive Treatment | STANNOUS FLUORIDE | Premier Dental Products Company | 04c3f178-7905-404d-9ac2-67c453287ddf | 2026-01-13 | Warnings | 48783-500-40 48783-500 48783050040 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.