NDC11 60687082732
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 |
|---|---|
| 60687-0827-32 | 60687-0827 |
| 60687-827-32 | 60687-827 |
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 |
|---|---|---|---|---|---|---|
| Lubiprostone | LUBIPROSTONE | American Health Packaging | 3014dd6d-9c05-479d-b79d-7a49f78a1ce5 | 2026-03-24 | Warnings, Adverse reactions | 60687-827-32 60687-827 60687082732 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.