For all supplies of medicinal products to a person authorized or entitled to supply medicinal products to the public in the Member State concerned, the authorized wholesaler must enclose a document that makes it possible to ascertain:

• the date,

• F1the name and pharmaceutical form of the medicinal product,

• the quantity supplied,

• the name and address of the supplier and consignorF3,

• F2batch number of the medicinal products at least for products bearing the safety features referred to in point (o) of Article 54.

Member States shall take all appropriate measures to ensure that persons authorized or entitled to supply medicinal products to the public are able to provide information that makes it possible to trace the distribution path of every medicinal product.