NDC11 00409516001
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 |
|---|---|
| 00409-5160-01 | 00409-5160 |
| 00409-5160-1 | 00409-5160 |
| 0409-5160-01 | 0409-5160 |
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 bromide | ROCURONIUM BROMIDE | Hospira, Inc. | f01f9986-43f9-40e8-9506-11bfe78f9242 | 2023-08-29 | Warnings, Adverse reactions | 0409-5160-01 0409-5160 00409516001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.