NDC11 70518406500
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 |
|---|---|
| 70518-4065-0 | 70518-4065 |
| 70518-4065-00 | 70518-4065 |
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 | REMEDYREPACK INC. | 9df3a51c-1b89-4d2a-8f41-3755910e9bfb | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | 70518-4065-0 70518-4065 70518406500 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.