NDC11 69543010750
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 |
|---|---|
| 69543-0107-50 | 69543-0107 |
| 69543-107-50 | 69543-107 |
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 |
|---|---|---|---|---|---|---|
| Desloratadine | DESLORATADINE | Virtus Pharmaceuticals, LLC | 0fe374d0-c14b-4102-b568-eb79165fc7ef | 2025-07-10 | Warnings, Adverse reactions | 69543-107-50 69543-107 69543010750 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.