Product Details for: Tevimbra

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
100MG/10ML (10MG/ML)
Single-Dose Vial
351(a)
Tevimbra
Rx
Proper Name
tislelizumab-jsgr
BLA Number
761232
Applicant
BeiGene USA, Inc.
Original Approval Date
March 13, 2024
Date of First Licensure