NDC11 59651020623
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 |
|---|---|
| 59651-0206-23 | 59651-0206 |
| 59651-206-23 | 59651-206 |
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 |
|---|---|---|---|---|---|---|
| Nitrofurantoin | NITROFURANTOIN | Aurobindo Pharma Limited | e9d10eaa-cf9c-469e-82ef-5af7285f2c86 | 2024-03-15 | Warnings, Adverse reactions | 59651-206-23 59651-206 59651020623 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.