NDC11 51672126202
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 |
|---|---|
| 51672-1262-02 | 51672-1262 |
| 51672-1262-2 | 51672-1262 |
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 |
|---|---|---|---|---|---|---|
| Desoximetasone | DESOXIMETASONE | Sun Pharmaceutical Industries, Inc. | 627031fc-9b91-4854-b08f-f9fc0c73f1de | 2025-07-03 | Warnings, Adverse reactions | 51672-1262-2 51672-1262 51672126202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.