NDC 50242-138

Actemra 162 mg per 0.9 mL injection, solution

On the label: Genentech, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Genentech, Inc.Oceanside, CA, United StatesMakes the active ingredient and tests it No problems foundAug 16, 2024 · 5 inspections
F. Hoffmann-La Roche AGKaiseraugst, SwitzerlandTests it, packages it and labels it Problems found, fixed voluntarilyMar 21, 2025 · 8 inspections
Roche Diagnostics GmbHMannheim, GermanyTests it, packages it and labels it Problems found, fixed voluntarilyOct 29, 2021 · 5 inspections
Roche Diagnostics GmbHPenzberg, GermanyTests it Problems found, fixed voluntarilyMay 22, 2025 · 6 inspections

Product details

Generic drug
Tocilizumab: every company that makes it
Form
injection, solution, subcutaneous
Strength
162 mg per 0.9 mL
Approval
BLA BLA125472
On the market since
Oct 21, 2013
Package NDCs
50242-138-01 50242-138-86
Official label
DailyMed (National Library of Medicine), updated Dec 16, 2025

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