NDC11 81643927001
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 |
|---|---|
| 81643-9270-01 | 81643-9270 |
| 81643-9270-1 | 81643-9270 |
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 |
|---|---|---|---|---|---|---|
| Floxuridine | FLOXURIDINE | JND Therapeutics, Inc. | 4681f23e-6b5e-433b-b245-3d0b4e64ebb2 | 2024-10-07 | Boxed warning, Warnings, Adverse reactions | 81643-9270-1 81643-9270 81643927001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.