NDC11 48783011208
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 |
|---|---|
| 48783-0112-08 | 48783-0112 |
| 48783-0112-8 | 48783-0112 |
| 48783-112-08 | 48783-112 |
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 |
|---|---|---|---|---|---|---|
| Monsels Solution | FERRIC SUBSULFATE | Premier Dental Products Company | 7a9923af-b8ed-4dc5-b6ae-2f42f83eb3db | 2026-01-13 | 48783-112-08 48783-112 48783011208 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.