NDC11 80513010525
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 |
|---|---|
| 80513-0105-25 | 80513-0105 |
| 80513-105-25 | 80513-105 |
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 |
|---|---|---|---|---|---|---|
| SENNA-S | DOCUSATE SODIUM AND SENNOSIDES | Advanced Rx LLC | d148be81-79b4-41f7-b8d8-a0e85b661592 | 2026-02-18 | Warnings | 80513-105-25 80513-105 80513010525 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.