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
Subcutaneous
162MG/0.9ML
Pre-Filled Syringe
351(a)
Actemra
Rx
002
Injection
Subcutaneous
162MG/0.9ML
Autoinjector
351(a)
Actemra
Rx
Proper Name
tocilizumab
BLA Number
125472
Applicant
Genentech, Inc.
Original Approval Date
October 21, 2013
Date of First Licensure
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