NDC11 71335201708
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 |
|---|---|
| 71335-2017-08 | 71335-2017 |
| 71335-2017-8 | 71335-2017 |
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 | Bryant Ranch Prepack | 3fbdcc34-6166-4843-839c-33fed718ffb2 | 2024-08-07 | Boxed warning, Warnings, Adverse reactions | 71335-2017-8 71335-2017 71335201708 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.