NDC11 65219020005
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 |
|---|---|
| 65219-0200-05 | 65219-0200 |
| 65219-0200-5 | 65219-0200 |
| 65219-200-05 | 65219-200 |
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 |
|---|---|---|---|---|---|---|
| Temsirolimus | TEMSIROLIMUS | Fresenius Kabi USA, LLC | 1c207bed-10e3-46f0-ad2c-69d5e5c97736 | 2020-03-30 | Warnings, Adverse reactions | 65219-200-05 65219-200 65219020005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.