When a medicinal product or product subject to the marketing authorisation provided for in Article L. 5121-8, to registration as a traditional herbal medicinal product or to registration as a homeopathic medicinal product is marketed, the company operating the medicinal product or product must notify the Agence nationale de sécurité du médicament et des produits de santé without delay of the marketing dates for each presentation of the medicinal product or product.