NDC11 82009005710
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 |
|---|---|
| 82009-0057-10 | 82009-0057 |
| 82009-057-10 | 82009-057 |
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 |
|---|---|---|---|---|---|---|
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | QUALLENT PHARMACEUTICALS HEALTH LLC | cb4c04a6-47d1-44ff-8d58-718102fa08eb | 2024-05-24 | Boxed warning, Warnings, Adverse reactions | 82009-057-10 82009-057 82009005710 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.