NDC11 51672402602
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 |
|---|---|
| 51672-4026-02 | 51672-4026 |
| 51672-4026-2 | 51672-4026 |
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 |
|---|---|---|---|---|---|---|
| Ketoconazole | KETOCONAZOLE | Sun Pharmaceutical Industries, Inc. | 8ca815a8-bccb-4ee2-a042-922373329cae | 2025-09-02 | Boxed warning, Warnings, Adverse reactions | 51672-4026-2 51672-4026 51672402602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.