NDC11 51662154201
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 |
|---|---|
| 51662-1542-01 | 51662-1542 |
| 51662-1542-1 | 51662-1542 |
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 | HF Acquisition Co LLC, DBA HealthFirst | dc43b289-4f32-1c1e-e053-2995a90a3a23 | 2022-04-09 | Warnings, Adverse reactions | 51662-1542-1 51662-1542 51662154201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.