NDC11 63402030430
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 |
|---|---|
| 63402-0304-30 | 63402-0304 |
| 63402-304-30 | 63402-304 |
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 |
|---|---|---|---|---|---|---|
| Latuda | LURASIDONE HYDROCHLORIDE | Sumitomo Pharma America, Inc. | afad3051-9df2-4c54-9684-e8262a133af8 | 2025-01-31 | Boxed warning, Warnings, Adverse reactions | 63402-304-30 63402-304 63402030430 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.