NDC11 47335057981
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 |
|---|---|
| 47335-0579-81 | 47335-0579 |
| 47335-579-81 | 47335-579 |
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 |
|---|---|---|---|---|---|---|
| Lurasidone Hydrochloride | LURASIDONE HYDROCHLORIDE | Sun Pharmaceutical Industries, Inc. | 6d97d871-66d3-4ed8-bbc5-0620e9f69ae5 | 2026-06-01 | Boxed warning, Warnings, Adverse reactions | 47335-579-81 47335-579 47335057981 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.