NDC11 59640069901
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 |
|---|---|
| 59640-0699-01 | 59640-0699 |
| 59640-0699-1 | 59640-0699 |
| 59640-699-01 | 59640-699 |
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 | OMEPRAZOLE | H E B | 4eb05eb3-be59-4132-95a8-5a8f5065d758 | 2026-08-10 | Warnings | 59640-699-01 59640-699 59640069901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.