Without prejudice to the provisions of 2° of Article R. 5121-50, each year the Agence nationale de sécurité du médicament et des produits de santé publishes on its website the list of medicinal products or products for which marketing authorisations have been refused, withdrawn or suspended in France, the supply of which has been prohibited or which have been withdrawn from the market, stating the reasons for these measures.
It also makes available on its website the list of medicinal products, published each year by the European Medicines Agency, for which marketing authorisations have been refused, withdrawn or suspended in the European Union, the supply of which has been prohibited or which have been withdrawn from the market.