NDC11 87441006601
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 |
|---|---|
| 87441-0066-01 | 87441-0066 |
| 87441-0066-1 | 87441-0066 |
| 87441-066-01 | 87441-066 |
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 Sodium | PANTOPRAZOLE SODIUM | Unit Dose Solutions, Inc. | 558dc7e1-dfd5-d3d7-e063-6394a90ab9c3 | 2026-07-01 | Warnings, Adverse reactions | 87441-066-01 87441-066 87441006601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.