NDC11 37808073203
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 |
|---|---|
| 37808-0732-03 | 37808-0732 |
| 37808-0732-3 | 37808-0732 |
| 37808-732-03 | 37808-732 |
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 and sodium bicarbonate | OMEPRAZOLE, SODIUM BICARBONATE | H E B | ddc8d73f-f4a1-42a7-89ee-420346820f61 | 2025-11-03 | Warnings | 37808-732-03 37808-732 37808073203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.