NDC11 51655014952
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 |
|---|---|
| 51655-0149-52 | 51655-0149 |
| 51655-149-52 | 51655-149 |
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 | Northwind Health Company, LLC | d9ba6c65-22bd-10c4-e053-2995a90ada2e | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 51655-149-52 51655-149 51655014952 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.