NDC11 67046035503
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 |
|---|---|
| 67046-0355-03 | 67046-0355 |
| 67046-0355-3 | 67046-0355 |
| 67046-355-03 | 67046-355 |
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 | Coupler LLC | 5088d6cd-ec13-384d-e063-6394a90aee05 | 2026-04-28 | Boxed warning, Warnings, Adverse reactions | 67046-0355-3 67046-0355 67046035503 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.