委员会条例(EC) No 1662/2005,修订理事会条例(EC) No 953/2003的附录I ,该条例避免某些关键药物贸易转移到欧盟
技术法规类型:欧盟Eurlex法规 来源:tbtmap
EURLEX ID:32005R1662
OJ编号:OJ L 267, 12.10.2005, p. 19-21
中文标题:委员会条例(EC) No 1662/2005,修订理事会条例(EC) No 953/2003的附录I ,该条例避免某些关键药物贸易转移到欧盟
原文标题:Commission Regulation (EC) No 1662/2005 of 11 October 2005 amending Annex I of Council Regulation (EC) No 953/2003 to avoid trade diversion into the European Union of certain key medicines
分类:11.70.10_总则
文件类型:二级立法 Regulation|条例
生效日期:2005-10-13
废止日期:2058-12-31
法规全文:查看欧盟官方文件
32005R1662
Title and reference
Commission Regulation (EC) No 1662/2005 of 11 October 2005 amending Annex I of Council Regulation (EC) No 953/2003 to avoid trade diversion into the European Union of certain key medicines
OJ L 267, 12.10.2005, p. 19‘�1 (ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, NL, PL, PT, SK, SL, FI, SV)
CS DA DE EL EN ES ET FI FR HU IT LT LV NL PL PT SK SL SV
Text
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Dates
- of document: 11/10/2005
of effect: 13/10/2005; Entry into force Date pub. + 1 See Art 2
end of validity: 99/99/9999
Classifications
- EUROVOC descriptor:
medicament
discriminatory price
EC customs territory
export restriction
customs regulations - Directory code:
11.70.10.00 External relations / Development policy / General
- Subject matter:
Development cooperation, External relations
Miscellaneous information
- Author:
European Commission - Form:
Regulation
Relationship between documents
- Treaty:
European Community - Legal basis:
32003R0953 -A04P8
- Select all documents based on this document
- Amendment to:
32003R0953 Amendment Replacement Annex 1 from 13/10/2005
- Select all documents mentioning this document
Consolidated versions
- consolidation form:
02003R0953
Text
| Bilingual display: BG CS DA DE EL EN ES ET FI FR HU IT LT LV NL PL PT RO SK SL SV |
Commission Regulation (EC) No 1662/2005
of 11 October 2005
amending Annex I of Council Regulation (EC) No 953/2003 to avoid trade diversion into the European Union of certain key medicines
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Regulation (EC) No 953/2003 of 26 May 2003 to avoid trade diversion into the European Union of certain key medicines [1], and in particular Article 4(4) and (8) thereof,
Whereas:
(1) The Commission has received modified applications under Article 4 of Regulation (EC) No 953/2003 with respect to Epivir 150 mg × 60 and Combivir 300/150 mg × 60.
(2) The Commission has determined that the applications received fulfil the requirements set out in Regulation (EC) No 953/2003 in accordance with the procedure laid down in Article 5(2) of that Regulation.
(3) The applicants have been informed of the Commission decision to accept their applications.
(4) It is therefore necessary to replace Annex I to Regulation (EC) No 953/2003,
HAS ADOPTED THIS REGULATION:
Article 1
Annex I to Regulation (EC) No 953/2003 is replaced by the Annex to this Regulation.
Article 2
This regulation enters into force on the day following its publication in the Official Journal of the European Union.
It shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 11 October 2005.
For the Commission
Peter Mandelson
Member of the Commission
[1] OJ L 135, 3.6.2003, p. 5. Regulation as amended by Commission Regulation (EC) No 1876/2004 (OJ L 326, 29.10.2004, p. 22).
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ANNEX
Product | Manufacturer/exporter | Country of destination | Distinctive features | Date of approval | CN/TARIC code |
"TRIZIVIR 750 mg × 60 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | Afghanistan Angola Armenia Azerbaijan Bangladesh Benin Bhutan Botswana Burkina Faso Burundi Cambodia Cameroon Cape Verde Central African Republic Chad Comoros Congo C么te d‘橧voire Djibouti DR Congo East Timor Equatorial Guinea Eritrea Ethiopia Gambia Ghana Guinea Guinea Bissau Haiti Honduras India Indonesia Kenya Kiribati Korea (Dem Rep) Kyrgyz Republic Lao People‘檚 DR Lesotho Liberia Madagascar Malawi Maldives Mali Mauritania Moldova Mongolia Mozambique Myanmar Namibia Nepal Nicaragua Niger Nigeria Pakistan Rwanda Samoa Sao Tome and Principe Senegal Sierra Leone Solomon Islands Somalia South Africa Sudan Swaziland Tajikistan Tanzania Togo Tuvalu Uganda Vanuatu Yemen Zambia Zimbabwe | Distinctive access pack ‘�tri-lingual text | 19.4.2004 | 30049019 |
EPIVIR 150 mg × 60 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | Distinctive access pack ‘�tri-lingual text ‘�red tablets | | 30049019 |
RETROVIR 250 mg × 40 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | General export pack (blue) not used in EU. French hospital pack ‘�Francophone markets | 19.4.2004 | 30049019 |
RETROVIR 300 mg × 60 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | General export pack (blue) not used in EU. French hospital pack ‘�Francophone markets | 19.4.2004 | 30049019 |
RETROVIR 100 mg × 100 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | General export pack (blue) not used in EU. French hospital pack ‘�Francophone markets | 19.4.2004 | 30049019 |
COMBIVIR 300/150 mg × 60 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | Distinctive access pack ‘�tri-lingual text Bottle (rather than blister pack) "A22" embossed red tablets | | 30049019 |
EPIVIR ORAL SOLUTION 10 mg/ml 240 ml | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | Distinctive access pack ‘�tri-lingual text | 19.4.2004 | 30049019 |
ZIAGEN 300 mg × 60 | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | General export pack ‘�not used in EU. French hospital pack ‘�Francophone countries | 20.9.2004 | 30049019 |
RETROVIR ORAL SOLUTION 10 mg/ml 200 ml | GLAXO SMITH KLINE GSK House 980 Great West Road BRENTFORD, MIDDX TW8 9GS United Kingdom | Distinctive access pack Tri-lingual text | 20.9.2004 | 30049019 |
[1] Only if applicable."
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