Avsola

Infliximab-axxq · Amgen, Inc
PRESCRIPTION ONLY (USA)

Avsola ingredients

Active ingredientStrength
Infliximab100 mg/10mL

What Avsola is used for

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

Rheumatoid arthritis Remicade, in combination with methotrexate, is indicated for the reduction of signs and symptoms as well as the improvement in physical function in: adult patients with active disease when the response to disease-modifying antirheumatic drugs (DMARDs), including methotrexate, has been inadequate; adult patients with severe, active and progressive disease not previously treated with methotrexate or other DMARDs. In these patient populations, a reduction in the rate of the progression of joint damage, as measured by X-ray, has been demonstrated. Adult Crohn's disease Remicade is indicated for: treatment of moderately to severely active Crohn's disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and / or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies; t…

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

Key facts

Brand
Avsola
Generic name
Infliximab-axxq
Made by
Amgen, Inc
Forms
Injection, Powder, Lyophilized, For Solution
Given
Intravenous
Drug class
Tumor Necrosis Factor Blocker
FDA approval
Biologic licence (BLA) BLA761086
On the US market since
2019

Official information

In India

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 Avsola?

Avsola (Infliximab-axxq) is a specialist medicine made by Amgen, Inc, approved by the US FDA.

What are the ingredients of Avsola?

Avsola contains Infliximab (100 mg/10mL).

Is Avsola approved in Europe?

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

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.