NDC11 65219044702
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 |
|---|---|
| 65219-0447-02 | 65219-0447 |
| 65219-0447-2 | 65219-0447 |
| 65219-447-02 | 65219-447 |
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 |
|---|---|---|---|---|---|---|
| Etomidate | ETOMIDATE | Fresenius Kabi USA, LLC | d07efb9e-5264-461d-96d8-e11fa71c5751 | 2023-07-27 | Warnings, Adverse reactions | 65219-447-02 65219-447 65219044702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.