ACTEMRA (TOCILIZUMAB)
Summary
FDA approved ACTEMRA (TOCILIZUMAB) by GENENTECH. BLA (Biologic) approval (Labeling) on 2025-12-10. INJECTABLE, INTRAVENOUS, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
BLA125472-59
Action Date
2025-12-10
Status
Approved
Category
drug
Product Code
BLA (Biologic)
Product Description
ACTEMRA (generic: TOCILIZUMAB), INJECTABLE, INTRAVENOUS, SUBCUTANEOUS. Application: BLA125472
Company
Context & Analysis
GENENTECH has 6 FDA actions in our database.
Frequently Asked Questions
How often does GENENTECH have FDA actions?
GENENTECH has 6 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "BLA125472-59" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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