NDC11 00409020110
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 |
|---|---|
| 00409-0201-10 | 00409-0201 |
| 00409-201-10 | 00409-201 |
| 0409-0201-10 | 0409-0201 |
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 |
|---|---|---|---|---|---|---|
| Docetaxel | DOCETAXEL ANHYDROUS | Hospira, Inc. | a0ec4bcc-93ea-4c41-a4b6-95ec19491807 | 2024-08-22 | Boxed warning, Warnings, Adverse reactions | 0409-0201-10 0409-0201 00409020110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.