NDC11 81864010330
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 |
|---|---|
| 81864-0103-30 | 81864-0103 |
| 81864-103-30 | 81864-103 |
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 |
|---|---|---|---|---|---|---|
| Ojjaara | MOMELOTINIB | GlaxoSmithKline LLC | 4a672fd1-eb7b-4aa9-9b23-845e4b5dc400 | 2026-07-20 | Warnings, Adverse reactions | 81864-103-30 81864-103 81864010330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.