NDC11 67877041905
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 |
|---|---|
| 67877-0419-05 | 67877-0419 |
| 67877-0419-5 | 67877-0419 |
| 67877-419-05 | 67877-419 |
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 | Ascend Laboratories, LLC | 7402aa01-50de-46c8-a341-d30da5b32b1c | 2025-06-13 | Warnings, Adverse reactions | 67877-419-05 67877-419 67877041905 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.