Dayvigo(lemborexant)
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Reference price:
Manufacturer:
Eisai
Formulation:
TABLET
Validity period:
24 months
Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.

Dayvigo(lemborexant) Instructions:Uses,Dosage, Side Effects

Lemborexant is a novel dual orexin receptor antagonist developed and manufactured by Eisai, a Japanese pharmaceutical company, specifically for the treatment of insomnia characterized by difficulties with sleep onset or sleep maintenance. The drug competitively binds to orexin receptors OX1R and OX2R, inhibits the wake-promoting effect of orexins, thereby reducing arousal signals, increasing sleepiness, and helping patients restore normal sleep rhythms. 

Since its approval by the U.S. FDA for marketing in December 2019, Lemborexant has been successively approved in dozens of countries and regions, including Japan, Canada, Australia, and China Hong Kong, bringing new treatment options for insomnia patients worldwide. On May 27, 2025, Eisai announced that the marketing application for Lemborexant tablets had been approved by the National Medical Products Administration (NMPA) of China.

Generic name

Dayvigo(lemborexant)
English name
lemborexant
Alternative Names
Dayvigo
Drug prices
Indications

Indicated for the treatment of adult insomnia characterized by difficulties with sleep onset or sleep maintenance.

Therapeutic Target
OX1R,OX2R
Active Ingredients
lemborexant
Dosage form
TABLET
specifications
2.5mg*100 tablets/box
Description
Dosage and Administration

1. The usual starting dose for adults is 5 mg, taken orally once daily at bedtime. 

2. If the efficacy is insufficient and well-tolerated, the dose may be increased to 10 mg.

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