NDC11 58151012593
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 |
|---|---|
| 58151-0125-93 | 58151-0125 |
| 58151-125-93 | 58151-125 |
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 |
|---|---|---|---|---|---|---|
| Effexor XR | VENLAFAXINE HYDROCHLORIDE | Viatris Specialty LLC | c848a5d8-ba94-4c84-80e3-0bf35fb8e32e | 2023-08-15 | Boxed warning, Warnings, Adverse reactions | 58151-125-93 58151-125 58151012593 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.