NDC11 43068090712
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 |
|---|---|
| 43068-0907-12 | 43068-0907 |
| 43068-907-12 | 43068-907 |
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 |
|---|---|---|---|---|---|---|
| FANAPT | ILOPERIDONE | Vanda Pharmaceuticals Inc. | 33f60b40-3fca-11de-8f56-0002a5d5c51b | 2026-05-06 | Boxed warning, Warnings, Adverse reactions | 43068-907-12 43068-907 43068090712 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.