NDC11 71288070006
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 |
|---|---|
| 71288-0700-06 | 71288-0700 |
| 71288-0700-6 | 71288-0700 |
| 71288-700-06 | 71288-700 |
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 | Meitheal Pharmaceuticals Inc. | b23aa80e-2af2-4a66-92ed-b1c8863be704 | 2026-01-09 | Warnings, Adverse reactions | 71288-700 |
| Rocuronium Bromide | ROCURONIUM BROMIDE | Meitheal Pharmaceuticals Inc. | b9abaf64-760d-43e0-8669-a9ca70feab11 | 2023-05-09 | Warnings, Adverse reactions | 71288-700-06 71288-700 71288070006 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.