NDC11 27241009705
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 |
|---|---|
| 27241-0097-05 | 27241-0097 |
| 27241-0097-5 | 27241-0097 |
| 27241-097-05 | 27241-097 |
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 | Ajanta Pharma USA Inc. | 2dde979d-b6f8-41d1-96fb-325c75ea3a74 | 2025-08-29 | Boxed warning, Warnings, Adverse reactions | 27241-097-05 27241-097 27241009705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.