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Lithuanian

English

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Lithuanian

Lapkricio 8­10 d.

English

11-12 January

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

Lapkricio 8­10 d.

English

8-10 November

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2002 m. lapkricio 12 d.

English

12 November 2002 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2002 m. lapkricio 20 d.

English

20 November 2002

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 9
Quality:

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Lithuanian

1999 m. lapkricio 25 d.

English

25/11/1999 Renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2000 m. lapkricio 29 d.

English

29th November 2000.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2006 m. lapkricio 20 d.

English

V. on 20 November 2006.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2001 m. lapkricio 20 d.) , cia (LL:

English

20 November 2001) , here (ALL:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

kadangi Susitarimo II priedas buvo iš dalies pakeistas 1997 m. lapkricio 12 d. EEE jungtinio komiteto sprendimu Nr. 76/97 [1],

English

Whereas Annex II to the Agreement was amended by Decision of the EEA Joint Committee No 76/97 of 12 November 1997 (1);

Last Update: 2016-09-30
Subject: Unknown
Usage Frequency: 1
Quality:

Reference:

Lithuanian

Šios proceduros buvo pradetos 2004 m. lapkricio men.

English

Further to discussions at the CHMP October 2004 plenary meeting, the European Commission recommended that this public health issue on all aspects of cardiovascular safety including thrombotic events and cardio-renal events is the subject of Community referrals under Article 31 of Directive 2001/ 83/ EC, as amended regarding decentrally authorised products containing celecoxib, etoricoxib and lumiracoxib and subject to a review procedure under Article 18 of Council Regulation (EEC) No 2309/ 93, as amended regarding the centrally authorised products containing celecoxib (Onsenal), parecoxib (Dynastat/ Rayzon) and valdecoxib (Bextra/ Valdyn), which were started in November 2004.

Last Update: 2011-10-23
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1999 m. lapkricio 16 d.2003 m. sausio 15 d.10.

English

10 DATE OF REVISION 13/11/2007

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2002 m. lapkricio 12 d.Rinkodaros teiss atnaujinimo data:

English

12 November 2002 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

Numatoma, jog trcioji metin atnaujinta informacija bus pateikta 2007 m. lapkricio mn. kaip treciosios metins pakartotinio vertinimo ataskaitos dalis.

English

12 of the renewal application.The third annual update is expected as part of the third Annual Reassessment Report in November 2007.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2000 m. lapkricio 16 d.Paskutins perregistracijos data:

English

16 November 2000 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1997 m. lapkricio 17 d.Paskutinio rinkodaros teiss atnaujinimo data:

English

17 November 1997 Date of latest renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1995 m. lapkricio 27 d.Paskutinio perregistravimo data:

English

27 November 1995 Date of latest renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1995 lapkricio 30 Paskutinio atnaujinimo data:

English

30 November 1995 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2005 m. lapkricio 7 d.CHMP/408150/2005

English

7 November 2005 CHMP/408150/2005

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

Registravimo liudijimas Lansopon (15 mg ir 30 mg) is pradzi buvo suteiktas Hexal AG Suomijoje 2003 m. lapkricio 7 dien.

English

A Marketing Authorisation for Lansopon (15 mg and 30 mg) was previously granted to Hexal AG in Finland on 7 November 2003.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

Prasymas pateikti papildomos informacijos pateiktas 2006 m. lapkricio 16 d.

English

A Request for Supplementary Information was adopted on 16 November 2006.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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