NDC11 37808004525
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 |
|---|---|
| 37808-0045-25 | 37808-0045 |
| 37808-045-25 | 37808-045 |
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 |
|---|---|---|---|---|---|---|
| Once Daily Relief | OLOPATADINE HYDROCHLORIDE OPHTHALMIC SOLUTION | H E B | 0cb0bb66-def2-35d4-7fe0-987757095d08 | 2025-12-12 | Warnings | 37808-045-25 37808-045 37808004525 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.