Product Details for: Avtozma

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
80MG/4ML (20MG/ML)
Single-Dose Vial
351(k) Interchangeable
Avtozma
Rx
002
Injection
Intravenous
200MG/10ML (20MG/ML)
Single-Dose Vial
351(k) Interchangeable
Avtozma
Rx
003
Injection
Intravenous
400MG/20ML (20MG/ML)
Single-Dose Vial
351(k) Interchangeable
Avtozma
Rx
Proper Name
tocilizumab-anoh
Reference Product Proper Name
tocilizumab
Reference Product Properietary Name
Actemra
BLA Number
761420
Applicant
CELLTRION, Inc.
Original Approval Date
January 24, 2025
Date of First Licensure
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