NDC11 72189056830
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 |
|---|---|
| 72189-0568-30 | 72189-0568 |
| 72189-568-30 | 72189-568 |
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 |
|---|---|---|---|---|---|---|
| Omeprazole/Sodiium Bicarbonate | OMEPRAZOLE/SODIIUM BICARBONATE | Direct_rx | 1f7f63c1-17c2-9a05-e063-6394a90abc6f | 2024-08-12 | Warnings, Adverse reactions | 72189-568-30 72189-568 72189056830 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.