NDC11 00409110522
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 |
|---|---|
| 00409-1105-22 | 00409-1105 |
| 0409-1105-22 | 0409-1105 |
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 |
|---|---|---|---|---|---|---|
| Atracurium Besylate | ATRACURIUM BESYLATE | Hospira, Inc. | de1c2dcd-295b-47ce-b7a1-a8be59939a54 | 2023-11-23 | Warnings, Adverse reactions | 0409-1105-22 0409-1105 00409110522 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.