NDC11 59651082505
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 |
|---|---|
| 59651-0825-05 | 59651-0825 |
| 59651-0825-5 | 59651-0825 |
| 59651-825-05 | 59651-825 |
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 |
|---|---|---|---|---|---|---|
| CIMETIDINE | CIMETIDINE | Aurobindo Pharma Limited | ebd53065-c080-4045-a398-64d3f3b1460f | 2024-11-14 | Adverse reactions | 59651-825-05 59651-825 59651082505 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.