NDC11 63323042601
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 |
|---|---|
| 63323-0426-01 | 63323-0426 |
| 63323-0426-1 | 63323-0426 |
| 63323-426-01 | 63323-426 |
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 | f1933332-1ae0-4dc1-be4c-694849e6c9f9 | 2023-04-17 | Warnings, Adverse reactions | 63323-426-01 63323-426 63323042601 |
| Rocuronium | ROCURONIUM BROMIDE | Fresenius Kabi USA, LLC | fb9524b2-c353-4747-8954-7ca2529eabb2 | 2023-01-11 | Warnings, Adverse reactions | 63323-426 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.