Directive 2001/83/EC of the European Parliament and of the… Article 57

Article 57

Notwithstanding Article 60, Member States may require the use of certain forms of labelling of the medicinal product making it possible to ascertain: - the price of the medicinal product, - the reimbursement conditions of social security organizations, - the legal status for supply to the patient, in accordance with Title VI, - identification and authenticity.

Read the full instrument → · Read this in context: TITLE V — LABELLING AND PACKAGE LEAFLET →

Other provisions in TITLE V — LABELLING AND PACKAGE LEAFLET

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 57 of Directive 2001/83/EC of the European Parliament and of the… (LawPlayer, data as of 2026-07-04)

What to look at next

Directive 2001/83/EC of the European Parliament and of the…, full textChapter navigation and full text, so you can read this section in contextEuropean Union legislation EU Legal Acts by type and yearGrouped by instrument type and year of enactment, so you can find others of the same kindBrowse by type and year TITLE V — LABELLING AND PACKAGE LEAFLET — read this in contextThe surrounding text of the act in order, so you can see what comes before and afterChapters and sections