NDC11 00409018701
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 |
|---|---|
| 00409-0187-01 | 00409-0187 |
| 00409-0187-1 | 00409-0187 |
| 00409-187-01 | 00409-187 |
| 0409-0187-01 | 0409-0187 |
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 |
|---|---|---|---|---|---|---|
| GEMCITABINE | GEMCITABINE | Hospira, Inc. | a625c92b-c569-4b98-8d2e-2b3f5e12b34f | 2024-08-16 | Warnings, Adverse reactions | 0409-0187-01 0409-0187 00409018701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.