NDC11 46122073904
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 |
|---|---|
| 46122-0739-04 | 46122-0739 |
| 46122-0739-4 | 46122-0739 |
| 46122-739-04 | 46122-739 |
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 | AMERISOURCEBERGEN DRUG CORPORATION | 0521c51b-d113-7e35-f1a6-c4495a2bcfcc | 2026-04-17 | Warnings | 46122-739-04 46122-739 46122073904 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.