NDC11 72603028801
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 |
|---|---|
| 72603-0288-01 | 72603-0288 |
| 72603-0288-1 | 72603-0288 |
| 72603-288-01 | 72603-288 |
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 | Northstar Rx LLC | 1626ac65-ea12-421b-9780-bfdb50a39e1a | 2025-06-25 | Warnings, Adverse reactions | 72603-288-01 72603-288 72603028801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.