NDC11 65862037410
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 |
|---|---|
| 65862-0374-10 | 65862-0374 |
| 65862-374-10 | 65862-374 |
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 |
|---|---|---|---|---|---|---|
| Escitalopram | ESCITALOPRAM OXALATE | Aurobindo Pharma Limited | d5fbc8ce-bd41-4bd0-b413-0dea97e596c3 | 2026-05-12 | Boxed warning, Warnings, Adverse reactions | 65862-374-10 65862-374 65862037410 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.