Vivanza

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Withdrawn

This medicine's authorisation has been withdrawn

vardenafil
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 3 February 2022, the European Commission withdrew the marketing authorisation for Vivanza (vardenafil) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Bayer AG, which notified the European Commission of its decision not to market the product in the EU for commercial reasons. 

Vivanza was granted marketing authorisation in the EU on 4 March 2003 for the treatment of erectile dysfunction. The marketing authorisation was initially valid for a 5-year period. It was then granted unlimited validity in 2007.The product had not been marketed in the EU since 2021. 

Vivanza was a duplicate of Levitra, which is marketed in several EU countries. The marketing authorisation holder will maintain the marketing authorisation for Levitra. 

The European Public Assessment Report (EPAR) for Vivanza is updated to indicate that the marketing authorisation is no longer valid.

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Product information

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Latest procedure affecting product information:N/0063
20/10/2021
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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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norsk (NO) (192.41 KB - PDF)

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Product details

Name of medicine
Vivanza
Active substance
vardenafil
International non-proprietary name (INN) or common name
vardenafil
Therapeutic area (MeSH)
Erectile Dysfunction
Anatomical therapeutic chemical (ATC) code
G04BE09

Pharmacotherapeutic group

Urologicals

Therapeutic indication

Treatment of erectile dysfunction in adult men. Erectile dysfunction is the inability to achieve or maintain a penile erection sufficient for satisfactory sexual performance.

In order for Vivanza to be effective, sexual stimulation is required.

Vivanza is not indicated for use by women.

Authorisation details

EMA product number
EMEA/H/C/000488
Marketing authorisation holder
Bayer AG 

51368 Leverkusen
Germany

Marketing authorisation issued
04/03/2003
Revision
28

Assessment history

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