Product Details for: Actemra
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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(a)
Actemra
Rx
002
Injection
Intravenous
200MG/10ML (20MG/ML)
Single-Dose Vial
351(a)
Actemra
Rx
003
Injection
Intravenous
400MG/20ML (20MG/ML)
Single-Dose Vial
351(a)
Actemra
Rx
Proper Name
tocilizumab
tocilizumab
BLA Number
125276
125276
Applicant
Genentech, Inc.
Genentech, Inc.
Original Approval Date
January 8, 2010
January 8, 2010
Date of First Licensure