NDC11 31722074931
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 |
|---|---|
| 31722-0749-31 | 31722-0749 |
| 31722-749-31 | 31722-749 |
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 |
|---|---|---|---|---|---|---|
| Linezolid | LINEZOLID | Camber Pharmaceuticals, Inc. | b239458e-9a3e-49ac-9ac7-a4badc53dff6 | 2025-01-09 | Warnings, Adverse reactions | 31722-749-31 31722-749 31722074931 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.