NDC11 80425014601
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 |
|---|---|
| 80425-0146-01 | 80425-0146 |
| 80425-0146-1 | 80425-0146 |
| 80425-146-01 | 80425-146 |
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 |
|---|---|---|---|---|---|---|
| Duloxetine HCL DR | DULOXETINE HCL | Advanced Rx Pharmacy of Tennessee, LLC | c4fa1d3b-f136-e14f-e053-2a95a90a6cfb | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 80425-0146-1 80425-0146 80425014601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.