NDC11 52389065601
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 |
|---|---|
| 52389-0656-01 | 52389-0656 |
| 52389-0656-1 | 52389-0656 |
| 52389-656-01 | 52389-656 |
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 |
|---|---|---|---|---|---|---|
| Diurex Ultimate | CAFFEINE | Kobayashi Healthcare International, Inc. | c6debbfe-6061-463f-8f17-fb240c6f1bab | 2026-06-08 | Warnings | 52389-656-01 52389-656 52389065601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.