Overview

The marketing authorisation for Vaxzevria (SRD) has been withdrawn at the request of the marketing-authorisation holder.

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Product information

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Latest procedure affecting product information: II/0096

07/03/2024

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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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svenska (SV) (32.46 KB - PDF)

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Product details

Name of medicine
Vaxzevria (previously COVID-19 Vaccine AstraZeneca)
Active substance
ChAdOx1-SARS-COV-2
International non-proprietary name (INN) or common name
COVID-19 Vaccine (ChAdOx1-S [recombinant])
Therapeutic area (MeSH)
COVID-19 virus infection
Anatomical therapeutic chemical (ATC) code
J07BN02

Pharmacotherapeutic group

Vaccines

Therapeutic indication

Vaxzevria is indicated for active immunisation to prevent COVID 19 caused by SARS CoV 2, in individuals 18 years of age and older.

The use of this vaccine should be in accordance with official recommendations.

Authorisation details

EMA product number
EMEA/H/C/005675
Marketing authorisation holder
AstraZeneca AB

151 85 Sodertalje
Sweden

Opinion adopted
29/01/2021
Marketing authorisation issued
29/01/2021
Withdrawal of marketing authorisation
27/03/2024
Revision
32

Assessment history

Safety updates

News on Vaxzevria (previously COVID-19 Vaccine AstraZeneca)

This page was last updated on

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