NDC11 61314014305
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 |
|---|---|
| 61314-0143-05 | 61314-0143 |
| 61314-0143-5 | 61314-0143 |
| 61314-143-05 | 61314-143 |
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 | dfd85672-fa4b-40e3-ac9c-81b8d9e4ffde | 2025-05-30 | Warnings, Adverse reactions | 61314-143-05 61314-143 61314014305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.