NDC11 00409409201
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 |
|---|---|
| 00409-4092-01 | 00409-4092 |
| 00409-4092-1 | 00409-4092 |
| 0409-4092-01 | 0409-4092 |
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 |
|---|---|---|---|---|---|---|
| COPPER | CUPRIC CHLORIDE | Hospira, Inc. | a84d61a4-8e7f-4be1-aba6-f633b334aafc | 2026-05-18 | Warnings, Adverse reactions | 0409-4092-01 0409-4092 00409409201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.