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Document 52004XC1029(02)

    Summary of Community decisions on marketing authorizations in respect of medicinal products from 15 September 2004 to 15 October 2004(Published pursuant to Article 12 or Article 34 of Council Regulation (EEC) No 2309/93)

    OJ C 266, 29.10.2004, p. 5–7 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)

    29.10.2004   

    EN

    Official Journal of the European Union

    C 266/5


    Summary of Community decisions on marketing authorizations in respect of medicinal products from 15 September 2004 to 15 October 2004

    (Published pursuant to Article 12 or Article 34 of Council Regulation (EEC) No 2309/93 (1))

    (2004/C 266/04)

    Issuing of a marketing authorisation (Article 12 of Council Regulation (EEC) No 2309/93): Accepted

    Date of the decision

    Name of the medicinal product

    Holder of the marketing authorisation

    Number of the entry in the Community Register

    Date of notification

    20.9.2004

    Angiox

    The Medicines Company UK Ltd, Suite B, Park House, 11 Milton Park, Abingdon, Oxfordshire OX14 4RS, United Kingdom

    EU/1/04/289/001

    22.9.2004

    20.9.2004

    Alimta

    Eli Lilly Nederland BV, Grootslag 1-5, 3991 RA Houten, Nederland

    EU/1/04/290/001

    22.9.2004

    20.9.2004

    Raptiva

    Serono Europe Limited, 56, Marsh Wall, London E14 9TP, United Kingdom

    EU/1/04/291/001-002

    22.9.2004

    21. 9.2004

    Protelos

    Les Laboratoires Servier, 22, rue Garnier, F-92200 Neuilly-sur-Seine

    EU/1/04/288/001-006

    23.9.2004

    21. 9.2004

    Osseor

    Les Laboratoires Servier, 22, rue Garnier, F-92200 Neuilly-sur-Seine

    EU/1/04/287/001-006

    23.9.2004

    27. 9.2004

    Apidra

    Aventis Pharma Deutschland GmbH, Brueningstrasse 50, D-65926 Frankfurt am Main,

    EU/1/04/285/001-020

    29. 9.2004

    13.10.2004

    Wilzin

    Orphan Europe SARL, Immeuble ‘Le Guillaumet’ F-92046 Paris-La-Défense

    EU/1/04/286/001-002

    18.10.2004

    Modification of a marketing authorisation (Article 12 of Council Regulation (EEC) No 2309/93) Accepted

    Date of the decision

    Name of the medicinal product

    Holder of the marketing authorisation

    Number of the entry in the Community Register

    Date of notification

    20.9.2004

    Remicade

    Centocor BV, Einsteinweg 101, 2333 CB Leiden, Nederland

    EU/1/99/116/001-003

    22.9.2004

    20.9.2004

    Azomyr

    Schering Plough Europe, Rue de Stalle, 73, B-1180 Brussels

    EU/1/00/157/014-021

    22.9.2004

    20.9.2004

    Aerius

    Schering Plough Europe, Rue de Stalle, 73, B-1180 Brussels

    EU/1/00/160/014-021

    22.9.2004

    20.9.2004

    Neoclarityn

    Schering Plough Europe, Rue de Stalle, 73, B-1180 Brussels,

    EU/1/00/161/014-021

    22.9.2004

    20.9.2004

    Lantus

    Aventis Pharma Deutschland GmbH, D-65926 Frankfurt am Main,

    EU/1/00/134/008-011

    EU/1/00/134/018-021

    22.9.2004

    20.9.2004

    Velcade

    Millennium Pharmaceuticals, Ltd, Building 3, Chiswick Park, 566 Chiswick High Road, Chiswick, London, W4 5YA United Kingdom

    EU/1/04/274/001

    22.9.2004

    20.9.2004

    Velcade

    Janssen-Cilag International NV, Turnhoutsewe 30, B–2340 Beerse

    EU/1/04/274/001

    23.9.2004

    20.9.2004

    Ovitrelle

    Serono Europe Limited, 56, Marsh Wall, London E14 9TP, United Kingdom

    EU/1/00/165/001-007

    22.9.2004

    21.9.2004

    Carbaglu

    Orphan Europe, Immeuble ‘Le Guillaumet’, F-92046 Paris-La-Défense

    EU/1/02/246/001-002

    23.9.2004

    21.9.2004

    KOGENATE Bayer

    Bayer AG, D-51368 Leverkusen, Deutschland

    EU/1/00/143/004-006

    23.9.2004

    23.9.2004

    Remicade

    Centocor B.V., Einsteinweg 101, 2333 CB Leiden, Nederland

    EU/1/99/116/001-003

    27.9.2004

    24.9.2004

    Insuman

    Aventis Pharma Deutschland GmbH, Brueningstrasse 50, D-65926 Frankfurt am Main,

    EU/1/97/030/065-084

    29.9.2004

    24.9.2004

    InductOs

    Wyeth Europa Ltd., Huntercombe Lane South, Taplow, Maidenhead, Berkshire, SL6 0PH, United Kingdom

    EU/1/02/226/001

    28.9.2004

    24.9.2004

    Enbrel

    Wyeth Europa Limited, Huntercombe Lane South, Taplow, Maidenhead, Berkshire, SL6 0PH, United Kingdom

    EU/1/99/126/001-003

    28.9.2004

    27.9.2004

    SonoVue

    Bracco International BV, Strawinskylaan 3051, 1077ZX Amsterdam, Nederland

    EU/1/01/177/001-002

    29.9.2004

    27.9.2004

    Ceprotin

    Baxter AG, Industriesstrasse 67, 1220 Vienna, Österreich

    EU/1/01/190/001-002

    29.9.2004

    27.9.2004

    Avonex

    Biogen Idec France, ‘Le Capitole’ 55, avenue des Champs Pierreux, F-92012 Nanterre Cedex

    EU/1/97/033/001-003

    30. 9.2004

    13.10.2004

    Revasc

    Canyon Pharmaceuticals Ltd, 20-22 Bedford Row - WC1R 4JS London - United Kingdom

    EU/1/97/043/001-002

    19.10.2004

    Aventis Pharma SA, 20 Avenue Raymond Aron, Antony Cedex F-92165

    18.10.2004

    13.10.2004

    Arava

    Aventis Pharma Deutschland GmbH, D-65926 Frankfurt am Main

    EU/1/99/118/001-010

    18.10.2004

    13.10.2004

    Vaniqa

    Shire Pharmaceutical Contracts Ltd, Hampshire International Business Park, Chineham, Basingstoke, Hampshire RG24 8EP, United Kingdom

    EU/1/01/173/001-003

    18.10.2004

    13.10.2004

    NovoRapid

    Novo Nordisk A/S, Novo Allé, DK-2880 Bagsvaerd

    EU/1/99/119/001-014

    18.10.2004

    13.10.2004

    Levviax

    Aventis Pharma SA, 20 Avenue Raymond Aron, F-92160 Antony

    EU/1/01/192/001-005

    19.10.2004

    15.10.2004

    Ketek

    Aventis Pharma SA, 20 Avenue Raymond Aron, F-92160 Antony

    EU/1/01/191/001-005

    19.10.2004

    15.10.2004

    Viramune

    Boehringer Ingelheim International GmbH, Binger Strasse, 173 D-55216 Ingelheim am Rhein, Deutschland

    EU/1/97/055/001-002

    19.10.2004

    15.10.2004

    Fuzeon

    Roche Registration Limited, 40 Broadwater Road, Welwyn Garden City, Hertfordshire AL7 3AY

    EU/1/03/252/001-003

    20.10.2004

    15.10.2004

    NovoRapid

    Novo Nordisk A/S, Novo Allé, DK-2880 Bagsvaerd

    EU/1/99/119/001

    EU/1/99/119/003

    EU/1/99/119/005-014

    19.10.2004

    Withdrawal of a marketing authorisation (Article 12 of Council Regulation (EEC) No 2309/93)

    Date of the decision

    Name of the medicinal product

    Holder of the marketing authorisation

    Number of the entry in the Community Register

    Date of notification

    28.9.2004

    Ixense

    Takeda Europe R&D Centre Ltd, Savanah House, 11/12 Charles II Street, London SW1Y 4QU, United Kingdom

    EU/1/01/181/001-007

    30.9.2004


    (1)   OJ L 214, 24.8.1993, p. 1.


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