NDC11 59651077601
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 |
|---|---|
| 59651-0776-01 | 59651-0776 |
| 59651-0776-1 | 59651-0776 |
| 59651-776-01 | 59651-776 |
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 |
|---|---|---|---|---|---|---|
| SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | Aurobindo Pharma Limited | 6f3145d7-f3c9-4456-a77d-d04c54f24668 | 2024-10-03 | Boxed warning, Warnings, Adverse reactions | 59651-776-01 59651-776 59651077601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.