Andexxa
Andexxa ingredients
| Active ingredient | Strength |
|---|---|
| Andexanet Alfa | 200 mg/20mL |
What Andexxa is used for
The FDA lists the approved uses on the official label (below). In the EU, andexanet alfa is approved as Ondexxya for:
For adult patients treated with a direct factor Xa (FXa) inhibitor (apixaban or rivaroxaban) when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding.
EU wording from the European Medicines Agency; US approved uses can differ.
Key facts
- Brand
- Andexxa
- Generic name
- Andexanet alfa
- Made by
- AstraZeneca Pharmaceuticals LP
- Forms
- Injection, Powder, Lyophilized, For Solution
- Given
- Intravenous
- FDA approval
- Biologic licence (BLA) BLA125586
- On the US market since
- 2022
Official information
- Andexxa prescribing information (FDA label) on DailyMed
- MedlinePlus drug information (search for Andexanet alfa)
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 Andexxa?
Andexxa (Andexanet alfa) is a specialist medicine made by AstraZeneca Pharmaceuticals LP, approved by the US FDA.
What are the ingredients of Andexxa?
Andexxa contains Andexanet Alfa (200 mg/20mL).
Is Andexxa approved in Europe?
The same active substance is approved in the EU as Ondexxya.
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