NDC11 61314014410
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 |
|---|---|
| 61314-0144-10 | 61314-0144 |
| 61314-144-10 | 61314-144 |
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 |
|---|---|---|---|---|---|---|
| Brimonidine Tartrate | BRIMONIDINE TARTRATE | Sandoz Inc | b1e7ebd4-d0d2-40a5-aa11-5f68bc5972bd | 2025-11-24 | Warnings, Adverse reactions | 61314-144-10 61314-144 61314014410 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.