NDC11 55150023502
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 |
|---|---|
| 55150-0235-02 | 55150-0235 |
| 55150-0235-2 | 55150-0235 |
| 55150-235-02 | 55150-235 |
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 |
|---|---|---|---|---|---|---|
| VECURONIUM BROMIDE | VECURONIUM BROMIDE | Eugia US LLC | 387b57ce-e50e-4e03-86d9-12638242bd36 | 2025-01-17 | Boxed warning, Warnings, Adverse reactions | 55150-235-02 55150-235 55150023502 |
| VECURONIUM BROMIDE | VECURONIUM BROMIDE | Eugia US LLC | 86d81719-534c-4e50-ae39-d8b20e50dfad | 2023-12-06 | Boxed warning, Warnings, Adverse reactions | 55150-235 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.