NDC11 63304004401
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 |
|---|---|
| 63304-0044-01 | 63304-0044 |
| 63304-0044-1 | 63304-0044 |
| 63304-044-01 | 63304-044 |
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 |
|---|---|---|---|---|---|---|
| Lenalidomide | LENALIDOMIDE | Sun Pharmaceutical Industries, Inc. | 84d9dec7-9250-4dbd-9a0d-23e75f111892 | 2024-12-13 | Boxed warning, Warnings, Adverse reactions | 63304-044-01 63304-044 63304004401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.