27.8.2004   

EN

Official Journal of the European Union

C 215/7


Summary of Community decisions on marketing authorizations in respect of medicinal products from 15 July 2004 to 15 August 2004

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

(2004/C 215/05)

Issuing of a marketing authorization (Article 12 of Council Regulation (EEC) No 2309/93  (1) ) Accepted

Date of the decision

Name of the medicinal product

Holder of the marketing authorization

Number of the entry in the Community Register

Date of notification

29.7.2004

Pedea

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

EU/1/04/284/001

2.8.2004

11.8.2004

Yentreve

Eli Lilly Nederland B.V., Grootslag 1-5, 3991 RA Houten, Nederland

EU/1/04/280/001-006.

13.8.2004

11.8.2004

Ariclaim

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

EU/1/04/283/001-006

13.8.2004

Modification of a marketing authorization (Article 12 of Council Regulation (EEC) No 2309/93  (1) ) Accepted

Date of the decision

Name of the medicinal product

Holder of the marketing authorization

Number of the entry in the Community Register

Date of notification

19.7.2004

Reyataz

Bristol - Myers Squibb Pharma EEIG, 141-149 Staines Road, Hounslow TW3 3JA, United Kingdom

EU/1/03/267/001-007

21.07.2004

19.7.2004

Humira

Abbott Laboratories Ltd., Queenborough, Kent ME11 5EL, United Kingdom

EU/1/03/256/001-006

21.07.2004

19.7.2004

Trudexa

Abbott Laboratories Ltd., Queenborough, Kent ME11 5EL, United Kingdom

EU/1/03/257/001-006

21.07.2004

19.7.2004

Nyracta

SmithKline Beecham plc, 980 Great West Road, Brentford, Middlesex, TW8 9GS United Kingdom

EU/1/00/139/001-012

21.07.2004

19.7.2004

Avandia

SmithKline Beecham plc, 980 Great West Road, Brentford, Middlesex, TW8 9GS United Kingdom

EU/1/00/137/001-012

21.07.2004

19.7.2004

Venvia

SmithKline Beecham plc, 980 Great West Road, Brentford, Middlesex, TW8 9GS United Kingdom

EU/1/00/138/001-012

21.07.2004

20.7.2004

Rebif

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

EU/1/98/063/001-006

23.07.2004

20.7.2004

Replagal

TKT Europe-5S AB, Rinkebyvägen 11B, SE 182 36 Danderyd, Sverige

EU/1/01/189/001-003

23.07.2004

20.7.2004

Refacto

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

EU/1/99/103/001-004

23.07.2004

22.7.2004

Mirapexin

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

Pfizer Enterprises SARL, 6, Circuit de la Foire Internationale, 1347 Luxembourg, Grand-Duché du Luxembourg

EU/1/97/051/001-006 EU/1/97/051/009-012

26.07.2004

23.7.2004

Enbrel

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

EU/1/99/126/001-003

27.07.2004

23.7.2004

Enbrel

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

EU/1/99/126/001-003

27.07.2004

29.7.2004

ReFacto

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

EU/1/99/103/001-004

2.8.2004

29.7.2004

Replagal

TKT Europe-5S AB, Rinkebyvägen 11B, SE 182 36 Danderyd, Sverige

EU/1/01/189/004-006

2.8.2004

2.8.2004

Procomvax

Aventis Pasteur MSD, 8, rue Jonas Salk, 69007 Lyon, France

EU/1/99/104/001

4.8.2004

2.8.2004

CoAprovel

Sanofi Pharma Bristol-Myers Squibb SNC, 174 avenue de France - 75013 Paris, France

EU/1/98/086/001-020

4.8.2004

2.8.2004

Aprovel

Sanofi Pharma Bristol-Myers Squibb SNC, 174 avenue de France - 75013 Paris, France

EU/1/97/046/001-030

4.8.2004

2.8.2004

Karvezide

Bristol-Myers Squibb Pharma EEIG, 141-149 Staines Road, Hounslow TW3 3JA - United Kingdom

EU/1/98/085/001-020

4.8.2004

2.8.2004

Karvea

Bristol-Myers Squibb Pharma EEIG, 141-149 Staines Road, Hounslow TW3 3JA - United Kingdom

EU/1/97/049/001-030

4.8.2004

2.8.2004

MabThera

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

EU/1/98/067/001-002

4.8.2004

2.8.2004

Plavix

Sanofi Pharma Bristol-Myers Squibb SNC, 174 avenue de France - 75013 Paris, France

EU/1/98/069/001a-001b, EU/1/98/069/002a-002b, EU/1/98/069/003a-003b, EU/1/98/069/004a-004b

4.8.2004

2.8.2004

Iscover

Bristol-Myers Squibb Pharma EEIG, 141-149 Staines Road, Hounslow TW3 3JA - United Kingdom

EU/1/98/070/001a-001b, EU/1/98/070/002a-002b, EU/1/98/070/003a-003b, EU/1/98/070/004a-004b

4.8.2004

2.8.2004

Prevenar

Wyeth-Lederle Vaccines S.A., Rue du Bosquet, 15 - 1348 Louvain-La-Neuve - Belgique

EU/1/00/167/001-007

4.8.2004

2.8.2004

Actrapid

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

EU/1/02/230/001-017

4.8.2004

2.8.2004

Mixtard

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

EU/1/02/231/001-037

4.8.2004

2.8.2004

Insulatard

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

EU/1/02/233/001-017

4.8.2004

2.8.2004

Velosulin

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

EU/1/02/232/001-003

4.8.2004

2.8.2004

Protaphane

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

EU/1/02/234/001-017

4.8.2004

2.8.2004

Puregon

Organon N.V., P.O. Box 20, 5340 BH Oss, Nederland

EU/1/96/008/038-039

4.8.2004

2.8.2004

Puregon,

Organon N.V., P.O. Box 20, 5340 BH Oss, Nederland

EU/1/96/008/040-041

4.8.2004

2.8.2004

Viread

Gilead Sciences International Limited, Cambridge CB1 6GT United Kingdom

EU/1/01/200/001

4.8.2004

2.8.2004

Emtriva

Gilead Sciences International Limited, Cambridge CB1 6GT United Kingdom

EU/1/03/261/001-003

4.8.2004

2.8.2004

Actraphane

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

EU/1/02/229/001-037

4.8.2004

2.8.2004

Norvir

Abbott laboratories Ltd, Queenborough, Kent ME11 5EL, United-Kingdom

EU/1/96/016/001 and EU/1/96/016/003

4.8.2004

2.8.2004

Starlix

Novartis Europharm Limited, Wimblehurst Road, Horsham, West Sussex RH12 5AB, United Kingdom

EU/1/01/174/001-021

4.8.2004

2.8.2004

Cellcept

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

EU/1/96/005/001-006

4.8.2004

2.8.2004

Protopy

Fujisawa GmbH, Neumarkter Str. 61, D-81673 München, Deutschland

EU/1/02/202/001-007

4.8.2004

2.8.2004

Inomax

INO Therapeutics AB, SE-181 81 Lidingö, Sverige

EU/1/01/194/001-002

4.8.2004

2.8.2004

Trazec

Novartis Europharm Limited, Wimblehurst Road, Horsham, West Sussex RH12 5AB, United Kingdom

EU/1/01/175/001-021

4.8.2004

4.8.2004

Insuman

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

EU/1/97/030/030, EU/1/97/030/035, EU/1/97/030/040, EU/1/97/030/045, EU/1/97/030/050, EU/1/97/030/055-064

6.8.2004

4.8.2004

Somavert

Pfizer Limited, Sandwich, Kent, CT13 9NJ, United Kingdom

EU/1/02/240/001-004

6.8.2004

9.8.2004

Fabrazyme

Genzyme Europe B.V., Gooimeer 10, Naarden 1411 DD, Nederland

EU/1/01/188/001-006

12.8.2004

11.8.2004

Vfend

Pfizer Limited, Sandwich, Kent CT13 9NJ, United Kingdom

EU/1/02/212/001-026

13.8.2004

12.8.2004

Infergen

Yamanouchi Europe B.V., Elisabethhof 19, NL-2353 EW Leiderdorp, Nederland

EU/1/98/087/001-003

16.8.2004

12.8.2004

Optison

Amersham Health AS, Nycoveien 1-2, P.O. Box 4220 Nydalen, 0401 Oslo, Norway

EU/1/98/065/001-002

16.8.2004

Modification of a marketing authorization (Article 34 of Council Regulation (EEC) No 2309/93  (1) ) Accepted

Date of the decision

Name of the medicinal product

Holder of the marketing authorization

Number of the entry in the Community Register

Date of notification

23.07.2004

Eurifel RCP FeL V

Merial, 29 avenue Tony Garnier, 69007 Lyon, France

EU/2/02/031/001-002

27.07.2004

29-07-2004

Virbagen Omega

VIRBAC S.A., 1ere Avenue 2065 m L.I.D. - 06516 Carros - France

EU/2/01/030/001-002

02-08-2004

11-08-2004

Porcilis Porcoli

Intervet International B.V. (NL), Wim de Körverstraat 35, 5831 AN Boxmeer, Nederland

EU/2/96/001/009-010

13-08-2004

Anyone wishing to consult the public assessment report on the medicinal products in question and the decisions relating thereto is invited to contact:

The European Agency for the Evaluation of Medicinal products

7, Westferry Circus, Canary Wharf

UK - LONDON E14 4HB


(1)  OJ L 214 of 24.8.1993, p. 1.