NDC11 76045022050
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 |
|---|---|
| 76045-0220-50 | 76045-0220 |
| 76045-220-50 | 76045-220 |
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 |
|---|---|---|---|---|---|---|
| Rocuronium | ROCURONIUM BROMIDE | Fresenius Kabi USA, LLC | 04c9812d-5aa3-4949-ad02-c618028f1bb0 | 2026-08-02 | Warnings, Adverse reactions | 76045-220-50 76045-220 76045022050 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.