Tyenne

Tocilizumab-aazg · Fresenius Kabi USA, LLC
PRESCRIPTION ONLY (USA)

Tyenne ingredients

Active ingredientStrength
Tocilizumab162 mg/.9mL, 80 mg/4mL, 200 mg/10mL, 400 mg/20mL

What Tyenne is used for

The FDA lists the approved uses on the official label (below). In the EU, tocilizumab is approved as RoActemra for:

RoActemra, in combination with methotrexate (MTX), is indicated for the treatment of severe, active and progressive rheumatoid arthritis (RA) in adults not previously treated with MTX. the treatment of moderate to severe active RA in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (DMARDs) or tumour necrosis factor (TNF) antagonists. In these patients, RoActemra can be given as monotherapy in case of intolerance to MTX or where continued treatment with MTX is inappropriate. RoActemra has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical function when given in combination with methotrexate. RoActemra is indicated for the treatment of active systemic juvenile idiopathic arthritis (sJIA) in patients 1 year of age and older, who…

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Tyenne
Generic name
Tocilizumab-aazg
Made by
Fresenius Kabi USA, LLC
Forms
Injection, Solution, Injection, Solution, Concentrate
Given
Intravenous, Subcutaneous
Drug class
Interleukin-6 Receptor Antagonist
FDA approval
Biologic licence (BLA) BLA761275
On the US market since
2024

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Tyenne?

Tyenne (Tocilizumab-aazg) is a specialist medicine made by Fresenius Kabi USA, LLC, approved by the US FDA.

What are the ingredients of Tyenne?

Tyenne contains Tocilizumab (162 mg/.9mL, 80 mg/4mL, 200 mg/10mL, 400 mg/20mL).

Is Tyenne approved in Europe?

The same active substance is approved in the EU as RoActemra.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.