NDC11 71288071205
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 |
|---|---|
| 71288-0712-05 | 71288-0712 |
| 71288-0712-5 | 71288-0712 |
| 71288-712-05 | 71288-712 |
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 |
|---|---|---|---|---|---|---|
| Cisatracurium Besylate | CISATRACURIUM BESYLATE | Meitheal Pharmaceuticals Inc. | 1be30efe-4beb-411a-bf82-6e4ea68fd262 | 2023-06-05 | Warnings, Adverse reactions | 71288-712 |
| Cisatracurium Besylate | CISATRACURIUM BESYLATE | Meitheal Pharmaceuticals Inc. | 7c8c41b6-d07c-4740-84b7-603289104c59 | 2023-01-19 | Warnings, Adverse reactions | 71288-712-05 71288-712 71288071205 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.