Product Details for: Leqembi IQLIK
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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
360MG/1.8ML (200MG/ML)
Autoinjector
351(a)
Leqembi IQLIK
Rx
002
Injection
Subcutaneous
250MG/1.25ML (200MG/ML)
Autoinjector
351(a)
Leqembi IQLIK
Rx
Proper Name
lecanemab-irmb
lecanemab-irmb
BLA Number
761375
761375
Applicant
Eisai, Incorporated
Eisai, Incorporated
Original Approval Date
August 29, 2025
August 29, 2025
Date of First Licensure