Opdivo

Nivolumab · E.R. Squibb & Sons, L.L.C.
CANCER MEDICINE · PRESCRIPTION ONLY (USA)

Opdivo ingredients

Active ingredientStrength
Nivolumab10 mg/mL

What Opdivo is used for

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

Melanoma Opdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older.Relative to nivolumab monotherapy, an increase in progression-free survival (PFS) and overall survival (OS) for the combination of nivolumab with ipilimumab is established only in patients with low tumour PD-L1 expression (see sections 4.4 and 5.1). Adjuvant treatment of melanoma Opdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with Stage IIB or IIC melanoma, or melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection (see section 5.1). Non-small cell lung cancer (NSCLC) Opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line tre…

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

Key facts

Brand
Opdivo
Generic name
Nivolumab
Made by
E.R. Squibb & Sons, L.L.C.
Forms
Injection
Given
Intravenous
Drug class
Programmed Death Receptor-1 Blocking Antibody
FDA approval
Biologic licence (BLA) BLA125554
On the US market since
2014

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 Opdivo?

Opdivo (Nivolumab) is a cancer medicine made by E.R. Squibb & Sons, L.L.C., approved by the US FDA.

What are the ingredients of Opdivo?

Opdivo contains Nivolumab (10 mg/mL).

Is Opdivo approved in Europe?

The same active substance is approved in the EU as Opdivo, Opdualag.

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.