NDC11 69584067210
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 |
|---|---|
| 69584-0672-10 | 69584-0672 |
| 69584-672-10 | 69584-672 |
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 |
|---|---|---|---|---|---|---|
| paroxetine hydrochloride | PAROXETINE HYDROCHLORIDE | Oxford Pharmaceuticals, LLC | 25182b68-8f7a-48e8-9788-6818b0984b29 | 2024-08-09 | Boxed warning, Warnings, Adverse reactions | 69584-672-10 69584-672 69584067210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.