NDC11 00078091195
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 |
|---|---|
| 00078-0911-95 | 00078-0911 |
| 00078-911-95 | 00078-911 |
| 0078-0911-95 | 0078-0911 |
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 |
|---|---|---|---|---|---|---|
| Xiidra | LIFITEGRAST | Novartis Pharmaceuticals Corporation | 8589d376-ac10-4ddb-9c53-2e0c8d5675c4 | 2025-08-18 | Adverse reactions | 0078-0911-95 0078-0911 00078091195 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.