NDC11 58602082605
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 |
|---|---|
| 58602-0826-05 | 58602-0826 |
| 58602-0826-5 | 58602-0826 |
| 58602-826-05 | 58602-826 |
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 |
|---|---|---|---|---|---|---|
| Acid Reducer | OMEPRAZOLE | Aurohealth LLC | 3eb70031-6439-44cf-8056-3e2e1e4a7fa9 | 2024-06-27 | Warnings | 58602-826-05 58602-826 58602082605 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.