NDC11 82950001201
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 |
|---|---|
| 82950-0012-01 | 82950-0012 |
| 82950-0012-1 | 82950-0012 |
| 82950-012-01 | 82950-012 |
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 |
|---|---|---|---|---|---|---|
| OJEMDA | TOVORAFENIB | Day One Biopharmaceuticals, Inc. | ea3a9631-3a66-6a7c-e053-2995a90ae2ad | 2025-09-02 | Warnings, Adverse reactions | 82950-012-01 82950-012 82950001201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.