# Directive 2009/35/EC of the European Parliament and of the Council of 23 April 2009 on the colouring matters which may be added to medicinal products (recast) (Text with EEA relevance), Part B

Extent: E+W+S+N.I.

List of time-limits for transposition into national law
(referred to in Article 7)
Pursuant to Article 7(2) of Directive 78/25/EEC: ‘2. However, any Member State may permit, on its own territory, until the end of a period of four years from the notification of this Directive, the marketing of medicinal products containing colouring matters which do not comply with the requirements of this Directive so long as these colouring matters were authorised in that Member State before the adoption of the Directive.’
Directive
Time-limit for transposition
78/25/EEC
15 June 1979
81/464/EEC
30 September 1981

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Source: https://www.legislation.gov.uk/eudr/2009/35/annex/I/part/B (the official version)
Page: https://openlegislation.uk/eu-directive-2009-35/annex-I/part-B
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.