NDC11 63187061260
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 |
|---|---|
| 63187-0612-60 | 63187-0612 |
| 63187-612-60 | 63187-612 |
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 | DULOXETINE HYDROCHLORIDE | Proficient Rx LP | c34f6115-f447-450f-8c83-58f3c51a76c9 | 2021-01-01 | Boxed warning, Warnings, Adverse reactions | 63187-612-60 63187-612 63187061260 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.