NDC11 85509133209
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 |
|---|---|
| 85509-1332-09 | 85509-1332 |
| 85509-1332-9 | 85509-1332 |
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 |
|---|---|---|---|---|---|---|
| Pantoprazole | PANTOPRAZOLE | PHOENIX RX LLC | 43fc6326-cfe6-7d1c-e063-6394a90abc24 | 2025-11-19 | Warnings, Adverse reactions | 85509-1332-9 85509-1332 85509133209 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.