NDC11 31722012590
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 |
|---|---|
| 31722-0125-90 | 31722-0125 |
| 31722-125-90 | 31722-125 |
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 | Camber Pharmaceuticals, Inc. | 8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd3 | 2021-10-29 | Boxed warning, Warnings, Adverse reactions | 31722-125-90 31722-125 31722012590 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.