NDC11 55150022110
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 |
|---|---|
| 55150-0221-10 | 55150-0221 |
| 55150-221-10 | 55150-221 |
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 | Eugia US LLC | 0820f15a-046b-4185-a2b3-2e4051ee3d82 | 2023-07-05 | Warnings, Adverse reactions | 55150-221-10 55150-221 55150022110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.