NDC11 44523074810
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 |
|---|---|
| 44523-0748-10 | 44523-0748 |
| 44523-748-10 | 44523-748 |
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 |
|---|---|---|---|---|---|---|
| SODIUM SULFACETAMIDE AND SULFUR | SODIUM SULFACETAMIDE 9.8% AND SULFUR 4.8% | BioComp Pharma, Inc. | 1ba8bb47-6f7a-28ec-e063-6394a90a8eb3 | 2025-06-05 | Warnings, Adverse reactions | 44523-748-10 44523-748 44523074810 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.