NDC11 57664068331
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 |
|---|---|
| 57664-0683-31 | 57664-0683 |
| 57664-683-31 | 57664-683 |
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 | Sun Pharmaceutical Industries, Inc. | 870c9600-04d5-4b44-a5b5-02252a310f22 | 2026-07-31 | Warnings, Adverse reactions | 57664-683-31 57664-683 57664068331 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.