NDC11 00065009265
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 |
|---|---|
| 00065-0092-65 | 00065-0092 |
| 00065-092-65 | 00065-092 |
| 0065-0092-65 | 0065-0092 |
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 |
|---|---|---|---|---|---|---|
| FLUORESCITE | FLUORESCEIN SODIUM | Alcon, Inc. | ebb3883c-71f6-4fd0-a7e6-0ba8e1136dd9 | 2026-06-29 | Warnings, Adverse reactions | 0065-0092-65 0065-0092 00065009265 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.