Boruzu

Bortezomib · Amneal Pharmaceuticals LLC
CANCER MEDICINE · PRESCRIPTION ONLY (USA)

Boruzu ingredients

Active ingredientStrength
Bortezomib3.5 mg/1.4mL

What Boruzu is used for

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

Velcade as monotherapy or in combination with pegylated liposomal doxorubicin or dexamethasone is indicated for the treatment of adult patients with progressive multiple myeloma who have received at least 1 prior therapy and who have already undergone or are unsuitable for haematopoietic stem cell transplantation. Velcade in combination with melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for high dose chemotherapy with haematopoietic stem cell transplantation. Velcade in combination with dexamethasone, or with dexamethasone and thalidomide, is indicated for the induction treatment of adult patients with previously untreated multiple myeloma who are eligible for high dose chemotherapy with haematopoietic stem cell transplantation. Velcade in combination with rituximab, cyclophosphamide, doxorubicin …

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

Key facts

Brand
Boruzu
Generic name
Bortezomib
Made by
Amneal Pharmaceuticals LLC
Forms
Injection
Given
Intravenous, Subcutaneous
Drug class
Proteasome Inhibitor
FDA approval
New drug application (NDA) NDA212782
On the US market since
2024

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 Boruzu?

Boruzu (Bortezomib) is a cancer medicine made by Amneal Pharmaceuticals LLC, approved by the US FDA.

What are the ingredients of Boruzu?

Boruzu contains Bortezomib (3.5 mg/1.4mL).

Is Boruzu approved in Europe?

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

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.