NDC11 81469029125
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 |
|---|---|
| 81469-0291-25 | 81469-0291 |
| 81469-291-25 | 81469-291 |
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 |
|---|---|---|---|---|---|---|
| Bimatoprost | BIMATOPROST | First Nation Group, LLC | 6a74ad65-dd76-45c1-9bbe-4218a9978b70 | 2026-04-08 | Warnings, Adverse reactions | 81469-291-25 81469-291 81469029125 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.