Hadlima

Adalimumab-bwwd · Organon LLC
PRESCRIPTION ONLY (USA)

Hadlima ingredients

Active ingredientStrength
Adalimumab40 mg/.8mL, 40 mg/.4mL

What Hadlima is used for

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

Please refer to the product information document.

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

Key facts

Brand
Hadlima
Generic name
Adalimumab-bwwd
Made by
Organon LLC
Forms
Solution
Given
Subcutaneous
Drug class
Tumor Necrosis Factor Blocker
FDA approval
Biologic licence (BLA) BLA761059
On the US market since
2023

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 Hadlima?

Hadlima (Adalimumab-bwwd) is a specialist medicine made by Organon LLC, approved by the US FDA.

What are the ingredients of Hadlima?

Hadlima contains Adalimumab (40 mg/.8mL, 40 mg/.4mL).

Is Hadlima approved in Europe?

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

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.