LEMBOREXANT - Food and Drug Administration

Manufacturer: Food and Drug Administration
Effective date: 2020-06-05
Label type: Indexing - product concept
Version: 1
Source: full-release
Hydrated at: 2026-06-05 00:18:59

Label at a glance#

ProductLEMBOREXANT

Active ingredientLEMBOREXANT

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

LEMBOREXANT

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LEMBOREXANT	0K5743G68X	ACTIB
LEMBOREXANT	0K5743G68X	ACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DAYVIGO	LEMBOREXANT	Eisai Inc.	7074cb65-77b3-45d2-8e8d-da8dc0f70bfd	2025-02-24	Warnings, Adverse reactions	Name fallback generic name: LEMBOREXANT

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.