NDC11 57664050083
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 |
|---|---|
| 57664-0500-83 | 57664-0500 |
| 57664-500-83 | 57664-500 |
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 |
|---|---|---|---|---|---|---|
| Mirtazapine | MIRTAZAPINE | Sun Pharmaceutical Industries, Inc. | f23631be-c7ae-46e9-b771-a70be17bc9f0 | 2021-11-30 | Boxed warning, Warnings, Adverse reactions | 57664-500-83 57664-500 57664050083 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.