NDC11 43598016360
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 |
|---|---|
| 43598-0163-60 | 43598-0163 |
| 43598-163-60 | 43598-163 |
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 | Dr. Reddy's Laboratories Inc. | 006b8b6c-f0eb-4246-87da-67582984b0e4 | 2026-07-10 | Warnings, Adverse reactions | 43598-163-60 43598-163 43598016360 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.