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Document E2014G1009(02)

    Läkemedel – Förteckningar över försäljningstillstånd som beviljats av Eftastaterna i EES under första halvåret 2012

    EUT C 356, 9.10.2014, p. 22–36 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    9.10.2014   

    SV

    Europeiska unionens officiella tidning

    C 356/22


    Läkemedel – Förteckningar över försäljningstillstånd som beviljats av Eftastaterna i EES under första halvåret 2012

    2014/C 356/07

    Underkommitté I – fri rörlighet för varor

    För gemensamma EES-kommitténs kännedom

    Med hänvisning till gemensamma ESS-kommitténs beslut nr 74/1999 av den 28 maj 1999 uppmanas gemensamma EES-kommittén att vid mötet den 15 juli 2013 notera följande förteckningar över försäljningstillstånd för läkemedel mellan den 1 januari och 30 juni 2012:

    Bilaga I

    Förteckning över nya försäljningstillstånd

    Bilaga II

    Förteckning över förlängda försäljningstillstånd

    Bilaga III

    Förteckning över utvidgade försäljningstillstånd

    Bilaga IV

    Förteckning över återkallade försäljningstillstånd

    Bilaga V

    Förteckning över upphävda försäljningstillstånd


    BILAGA I

    Förteckning över nya försäljningstillstånd

    Följande försäljningstillstånd har beviljats i Eftastaterna i EES mellan den 1 januari och 30 juni 2012:

    EU-nummer

    Produkt

    Land

    Datum för godkännande

    EU/1/11/711/001–030

    Matever

    Norge

    1.6.2012

    EU/1/11/712/001–028

    Levetiracetam Accord

    Norge

    13.4.2012

    EU/1/11/713/001–040

    Levetiracetam Actavis

    Norge

    16.4.2012

    EU/1/11/715/001–002

    Plenadren

    Island

    23.4.2012

    EU/1/11/721/001–021

    Paglitaz

    Norge

    13.4.2012

    EU/1/11/721/001–021

    Paglitaz

    Island

    17.4.2012

    EU/1/11/722/001–030

    Pioglitazone Accord

    Norge

    11.4.2012

    EU/1/11/722/001–030

    Pioglitazon Accord

    Liechtenstein

    30.4.2012

    EU/1/11/722/001–030

    Pioglitazone Accord

    Island

    20.4.2012

    EU/1/11/723/001–021

    Pioglitazone Krka

    Norge

    23.5.2012

    EU/1/11/723/001–021

    Pioglitazone Krka

    Island

    20.4.2012

    EU/1/11/727/001

    Mercatopurine Nova lab.

    Norge

    19.4.2012

    EU/1/11/727/001

    Mercaptopurine Nova Laboratories

    Island

    3.4.2012

    EU/1/11/727/001

    Mercatopurine Nova Laboratories

    Liechtenstein

    30.4.2012

    EU/1/11/729/001–006

    Onduarp

    Norge

    8.5.2012

    EU/1/11/730/001–060

    Rasitrio

    Island

    3.2.2012

    EU/1/11/738/001–003

    Levetiracetam Actavis Gr.

    Norge

    1.3.2012

    EU/1/11/739/001–008

    Dasselta

    Norge

    16.1.2012

    EU/1/11/740/001

    Ameluz

    Island

    5.1.2012

    EU/1/11/740/001

    Ameluz

    Norge

    16.1.2012

    EU/1/11/741/001

    Levetiracetam SUN

    Norge

    27.1.2012

    EU/1/11/741/001

    Levetiracetam Sun

    Island

    9.1.2012

    EU/1/11/742/001–010

    Efavirenz Teva

    Norge

    13.2.2012

    EU/1/11/742/001–010

    Efavirenz Teva

    Island

    24.1.2012

    EU/1/11/742/001–010

    Efavirenz Teva

    Liechtenstein

    29.2.2012

    EU/1/11/743/001–015

    Repaglinide Accord

    Norge

    13.2.2012

    EU/1/11/743/001–015

    Repaglinide Accord

    Island

    19.1.2012

    EU/1/11/743/001–015

    Repaglinide Accord

    Liechtenstein

    29.2.2012

    EU/1/11/744/001–002

    Topotecan Eagle

    Island

    22.1.2012

    EU/1/11/744/001–002

    Topotecan Eagle

    Liechtenstein

    29.2.2012

    EU/1/11/745/001–009

    Desloratadine Actavis

    Island

    3.2.2012

    EU/1/11/745/001–009

    Desloratadine Actavis

    Norge

    13.2.2012

    EU/1/11/746/001–012

    Desloratadine ratiopharm

    Norge

    13.2.2012

    EU/1/11/746/001–012

    Desloratadine ratiopharm

    Island

    3.2.2012

    EU/1/11/746/001–012

    Desloratadine ratiopharm

    Liechtenstein

    29.2.2012

    EU/1/11/747/001

    Colobreathe

    Island

    29.2.2012

    EU/1/11/747/001

    Colobreathe

    Liechtenstein

    29.2.2012

    EU/1/11/748/001–006

    Docetaxel Mylan

    Island

    7.2.2012

    EU/1/11/748/001–006

    Docetaxel Mylan

    Liechtenstein

    29.2.2012

    EU/1/11/749/001–002

    Caprelsa

    Liechtenstein

    30.4.2012

    EU/1/11/749/001–003

    Caprelsa

    Island

    9.3.2012

    EU/1/11/749/001–002

    Caprelsa

    Norge

    13.3.2012

    EU/1/12/750/001

    Esmya

    Norge

    30.3.2012

    EU/1/12/750/001

    Esmya

    Island

    14.3.2012

    EU/1/12/750/001

    Esmya

    Liechtenstein

    30.4.2012

    EU/1/12/751/001

    Zelboraf

    Norge

    14.3.2012

    EU/1/12/751/001

    Zelboraf

    Island

    7.3.2012

    EU/1/12/751/001

    Zelboraf

    Liechtenstein

    29.2.2012

    EU/1/12/752/001

    Vepacel

    Norge

    1.3.2012

    EU/1/12/752/001

    Vepacel

    Island

    9.3.2012

    EU/1/12/752/001

    Vepacel

    Liechtenstein

    29.2.2012

    EU/1/12/753/001–012

    Signifor

    Norge

    10.5.2012

    EU/1/12/753/001–012

    Signifor

    Island

    24.5.2012

    EU/1/12/753/001–012

    Signifor

    Liechtenstein

    30.6.2012

    EU/1/12/754/001–021

    Sepioglin

    Norge

    10.4.2012

    EU/1/12/754/001–021

    Sepioglin

    Island

    3.4.2012

    EU/1/12/754/001–021

    Sepioglin

    Liechtenstein

    30.4.2012

    EU/1/12/755/001–027

    Pioglitazone Actavis

    Norge

    13.4.2012

    EU/1/12/755/001–027

    Pioglitazone Actavis

    Island

    30.4.2012

    EU/1/12/756/001–027

    Glidipion (ex Ogliton)

    Norge

    13.4.2012

    EU/1/12/756/001–027

    Pioglitazone Actavis Group

    Island

    13.4.2012

    EU/1/12/756/001–027

    Pioglitazone Actavis Group

    Liechtenstein

    30.4.2012

    EU/1/12/757/001–030

    Pioglitazone Teva

    Norge

    11.4.2012

    EU/1/12/757/001–030

    Pioglitazone Teva

    Island

    23.4.2012

    EU/1/12/758/001–030

    Pioglitazone Teva Pharma

    Norge

    17.4.2012

    EU/1/12/758/001–030

    Pioglitazone Teva Pharma

    Island

    25.4.2012

    EU/1/12/759/001–003

    Zoledronic acid Actavis

    Norge

    8.5.2012

    EU/1/12/759/001–003

    Zoledronic acid Actavis

    Island

    16.5.2012

    EU/1/12/759/001–003

    Zoledronsäure Actavis

    Liechtenstein

    30.4.2012

    EU/1/12/760/001–002

    Bronchitol

    Norge

    18.5.2012

    EU/1/12/760/001–002

    Bronchitol

    Island

    9.5.2012

    EU/1/12/761/001–002

    Capecitabine Teva

    Norge

    30.5.2012

    EU/1/12/761/001–002

    Capecitabine Teva

    Island

    20.5.2012

    EU/1/12/761/001–002

    Capecitabin Teva

    Liechtenstein

    30.4.2012

    EU/1/12/762/001–018

    Capecitabine Accord

    Island

    20.5.2012

    EU/1/12/762/001–018

    Capecitabin Accord

    Liechtenstein

    30.4.2012

    EU/1/12/763/001–018

    Capecitabine Krka

    Island

    16.5.2012

    EU/1/12/763/001–018

    Capecitabin Krka

    Liechtenstein

    30.4.2012

    EU/1/12/763/001–018

    Capecitabine Krka

    Norge

    14.6.2012

    EU/1/12/764/001

    Pixuvri

    Norge

    14.6.2012

    EU/1/12/764/001

    Pixuvri

    Island

    29.5.2012

    EU/1/12/764/001

    Pixuvri

    Liechtenstein

    30.6.2012

    EU/1/12/765/001–004

    Sabervel

    Island

    9.5.2012

    EU/1/12/765/001–006

    Sabervel

    Norge

    8.5.2012

    EU/1/12/765/001–006

    Sabervel

    Liechtenstein

    30.4.2012

    EU/1/12/766/001

    Sancuso

    Norge

    10.5.2012

    EU/1/12/766/001

    Sancuso

    Island

    20.5.2012

    EU/1/12/766/001

    Sancuso

    Liechtenstein

    30.6.2012

    EU/1/12/767/001–007

    Nimenrix

    Norge

    1.5.2012

    EU/1/12/767/001–007

    Nimenrix

    Island

    16.5.2012

    EU/1/12/768/001

    Riluzole Zentiva

    Island

    25.5.2012

    EU/1/12/768/001

    Riluzol Zentiva

    Liechtenstein

    30.6.2012

    EU/1/12/769/001–003

    Docetaxel Accord

    Island

    12.6.2012

    EU/1/12/769/001–003

    Docetaxel Accord

    Liechtenstein

    30.6.2012

    EU/1/12/770/001–004

    Docetaxel Kabi

    Norge

    19.6.2012

    EU/1/12/770/001–004

    Docetaxel Kabi

    Island

    13.6.2012

    EU/1/12/770/001–004

    Docetaxel Kabi

    Liechtenstein

    30.6.2012

    EU/2/11/134/001–014

    Inflacam

    Norge

    6.1.2012

    EU/2/11/135/001–003

    Panacur AquaSol

    Norge

    10.2.2012

    EU/2/11/136/001

    Truscient

    Norge

    6.1.2012

    EU/2/11/136/001

    TruScient

    Island

    12.1.2012

    EU/2/11/137/001–015

    Activyl Tick Plus

    Norge

    13.2.2012

    EU/2/11/137/001–015

    Activyl Tick Plus

    Island

    25.1.2012

    EU/2/11/137/001–015

    Activyl Tick Plus

    Liechtenstein

    29.2.2012

    EU/2/12/138/001–003

    RevitaCAM

    Island

    14.3.2012

    EU/2/12/139/001–003

    Zulvac 1 + 8 Bovis

    Norge

    3.4.2012

    EU/2/12/139/001–003

    Zulvac 1 + 8 Bovis

    Island

    4.4.2012

    EU/2/12/139/001–003

    Zulvac 1 + 8 Bovis

    Liechtenstein

    30.4.2012


    BILAGA II

    Förteckning över förlängda försäljningstillstånd

    Följande försäljningstillstånd har förlängts i Efta-staterna i EES mellan den 1 januari och 30 juni 2012:

    EU-nummer

    Produkt

    Land

    Datum för godkännande

    EU/1/01/197/001–005

    Foscan

    Island

    14.5.2012

    EU/1/01/200/001–002

    Viread

    Norge

    6.1.2012

    EU/1/01/200/001–002

    Viread

    Island

    5.1.2012

    EU/1/02/209/001–008

    Dynastat

    Norge

    8.3.2012

    EU/1/02/209/001–008

    Dynastat

    Island

    7.2.2012

    EU/1/02/209/001–008

    Dynastat

    Liechtenstein

    29.2.2012

    EU/1/02/212/001–026

    Vfend

    Norge

    6.3.2012

    EU/1/02/212/001–026

    Vfend

    Island

    14.3.2012

    EU/1/02/212/001–026

    Vfend

    Liechtenstein

    30.4.2012

    EU/1/02/216/001–002

    Invanz

    Norge

    19.1.2012

    EU/1/02/216/001–002

    Invanz

    Island

    20.1.2012

    EU/1/02/216/001–002

    Invanz

    Liechtenstein

    29.2.2012

    EU/1/02/220/001–006

    Tracleer

    Norge

    8.5.2012

    EU/1/02/220/001–006

    Tracleer

    Island

    20.5.2012

    EU/1/02/220/001–006

    Tracleer

    Liechtenstein

    30.4.2012

    EU/1/02/222/001–005

    Tamiflu

    Norge

    8.3.2012

    EU/1/02/222/001–005

    Tamiflu

    Island

    19.6.2012

    EU/1/02/222/001–005

    Tamiflu

    Liechtenstein

    30.6.2012

    EU/1/06/334/001–005

    Evoltra

    Liechtenstein

    30.4.2012

    EU/1/06/347/001–008

    Sutent

    Liechtenstein

    29.2.2012

    EU/1/06/366/005–022

    Tandemact

    Norge

    11.4.2012

    EU/1/06/366/005–022

    Tandemact

    Island

    22.3.2012

    EU/1/06/366/005–022

    Tandemact

    Liechtenstein

    30.4.2012

    EU/1/06/367/001–012

    Diacomit

    Norge

    6.3.2012

    EU/1/06/367/001–012

    Diacomit

    Island

    7.2.2012

    EU/1/06/367/001–012

    Diacomit

    Liechtenstein

    29.2.2012

    EU/1/06/370/001–039

    Exforge

    Norge

    16.1.2012

    EU/1/06/370/001–039

    EXFORGE

    Island

    3.2.2012

    EU/1/06/371/001–039

    Dafiro

    Island

    8.2.2012

    EU/1/06/371/001–039

    Dafiro

    Liechtenstein

    29.2.2012

    EU/1/06/372/001–039

    Copalia

    Norge

    11.1.2012

    EU/1/06/373/001–039

    Imprida

    Norge

    16.1.2012

    EU/1/06/373/001–039

    Imprida

    Island

    6.2.2012

    EU/1/06/374/001

    Lucentis

    Norge

    17.1.2012

    EU/1/06/374/001

    Lucentis

    Island

    12.1.2012

    EU/1/06/376/001–033

    Irbesartan Zentiva (ex-Winthrop)

    Norge

    14.2.2012

    EU/1/06/376/001–033

    Irbesartan Zentiva

    Island

    7.2.2012

    EU/1/06/376/001–033

    Irbesartan Winthrop

    Liechtenstein

    29.2.2012

    EU/1/06/377/001–028

    Irbesartan HCT Zentiva (ex-Winthrop)

    Norge

    16.4.2012

    EU/1/06/377/001–028

    Irbesartan HCT Zentiva

    Island

    22.3.2012

    EU/1/06/377/001–028

    Irbesartan HCT

    Liechtenstein

    30.4.2012

    EU/1/06/378/001–017

    Inovelon

    Norge

    6.3.2012

    EU/1/06/378/001–017

    Inovelon

    Island

    24.1.2012

    EU/1/06/378/001–017

    Inovelon

    Liechtenstein

    29.2.2012

    EU/1/06/379/001

    Cystadane

    Island

    9.3.2012

    EU/1/06/379/001

    Cystadane

    Liechtenstein

    29.2.2012

    EU/1/06/386/001–015, 020–024, 029–033, 038–042, 047–051, 056–057, 088–102, 113–150, 163–168

    Insulin Human Winthrop

    Norge

    6.1.2012

    EU/1/07/382/001–018

    Xelevia

    Norge

    14.2.2012

    EU/1/07/382/001–018

    Xelevia

    Island

    6.2.2012

    EU/1/07/382/001–018

    Xelevia

    Liechtenstein

    29.2.2012

    EU/1/07/383/001–018

    Januvia

    Norge

    26.3.2012

    EU/1/07/383/001–018

    Januvia

    Island

    11.5.2012

    EU/1/07/383/001–018

    Januvia

    Liechtenstein

    30.4.2012

    EU/1/07/384/003–005

    Docetaxel Winthrop

    Norge

    10.4.2012

    EU/1/07/384/003–005

    Docetaxel Winthrop

    Island

    23.3.2012

    EU/1/07/384/003–005

    Docetaxel Winthrop

    Liechtenstein

    30.4.2012

    EU/1/07/386/001–018

    Toviaz

    Norge

    11.4.2012

    EU/1/07/386/001–018

    Toviaz

    Island

    10.4.2012

    EU/1/07/386/001–018

    Toviaz

    Liechtenstein

    30.4.2012

    EU/1/07/387/001–026

    Advagraf

    Norge

    2.5.2012

    EU/1/07/387/001–026

    Advagraf

    Island

    9.5.2012

    EU/1/07/387/001–026

    Advagraf

    Liechtenstein

    30.4.2012

    EU/1/07/388/001–003

    Sebivo

    Norge

    8.5.2012

    EU/1/07/388/001–003

    Sebivo

    Island

    16.5.2012

    EU/1/07/388/001–003

    Sebivo

    Liechtenstein

    30.4.2012

    EU/1/07/389/001–003

    Orencia

    Norge

    10.4.2012

    EU/1/07/389/001–003

    Orencia

    Island

    10.4.2012

    EU/1/07/389/001–003

    Orencia

    Liechtenstein

    30.4.2012

    EU/1/07/390/001–004

    Altargo

    Norge

    8.5.2012

    EU/1/07/390/001–004

    Altargo

    Island

    16.5.2012

    EU/1/07/390/001–004

    Altargo

    Liechtenstein

    30.4.2012

    EU/1/07/391/001–004

    Revlimid

    Norge

    3.5.2012

    EU/1/07/391/001–004

    Revlimid

    Island

    9.5.2012

    EU/1/07/391/001–004

    Revlimid

    Liechtenstein

    30.4.2012

    EU/1/07/392/001–003

    Circadin

    Norge

    16.5.2012

    EU/1/07/392/001–003

    Circadin

    Island

    10.5.2012

    EU/1/07/392/001–003

    Circadin

    Liechtenstein

    30.6.2012

    EU/1/07/394/001–009

    Optaflu

    Norge

    20.6.2012

    EU/1/07/395/001–095

    Invega

    Liechtenstein

    30.6.2012

    EU/1/07/396/001–003

    Pergoveris

    Island

    20.6.2012

    EU/1/07/396/001–003

    Pergoveris

    Liechtenstein

    30.6.2012

    EU/1/07/398/001–014

    Optimark

    Norge

    27.6.2012

    EU/1/07/399/001–006

    Aerinaze

    Norge

    18.6.2012

    EU/1/07/399/001–006

    Aerinaze

    Liechtenstein

    30.6.2012

    EU/1/07/399/001–006

    Aerinaze

    Island

    20.6.2012

    EU/1/07/400/008–013, 017–024

    Mircera

    Island

    7.6.2012

    EU/1/07/400/008–013, 017–024

    Mircera

    Norge

    14.6.2012

    EU/1/07/400/017–024

    Mircera

    Liechtenstein

    30.6.2012

    EU/1/07/401/007–016

    alli

    Norge

    29.6.2012

    EU/1/07/412/001–052

    Abseamed

    Liechtenstein

    30.6.2012

    EU/1/07/423/001–003

    Vectibix

    Norge

    19.3.2012

    EU/1/07/423/001–003

    Vectibix

    Island

    9.3.2012

    EU/1/07/440/001–003

    Tyverb

    Liechtenstein

    30.4.2012

    EU/1/07/440/001–006

    Tyverb

    Norge

    2.5.2012

    EU/1/07/440/001–006

    Tyverb

    Island

    11.5.2012

    EU/1/10/625/001&003

    Arzerra

    Island

    17.2.2012

    EU/1/10/625/001&003

    Arzerra

    Norge

    18.5.2012

    EU/1/10/628/001–004

    Votrient

    Norge

    19.6.2012

    EU/1/10/628/001–004

    Votrient

    Island

    13.6.2012

    EU/1/11/699/001–004

    Fampyra

    Norge

    19.6.2012

    EU/1/11/699/001–004

    Fampyra

    Island

    13.6.2012

    EU/1/11/699/001–004

    Fampyra

    Liechtenstein

    30.6.2012

    EU/2/05/053/001–003

    Naxcel

    Norge

    14.2.2012

    EU/2/06/068/001–004

    Ypozane

    Norge

    13.2.2012

    EU/2/06/068/001–004

    Ypozane

    Island

    18.1.2012

    EU/2/06/068/001–004

    Ypozane

    Liechtenstein

    30.4.2012

    EU/2/06/070/001–008

    Meloxidyl

    Island

    13.1.2012

    EU/2/07/071/001–003

    SLENTROL

    Island

    7.5.2012

    EU/2/07/071/001–003

    Slentrol

    Liechtenstein

    30.4.2012

    EU/2/07/072/001–004

    Suprelorin

    Island

    21.6.2012

    EU/2/07/074/001–006

    Prilactone

    Island

    13.6.2012

    EU/2/07/075/001–004

    Circovac

    Liechtenstein

    30.6.2012

    EU/2/07/075/001–004

    Circovac

    Island

    4.6.2012


    BILAGA III

    Förteckning över utvidgade försäljningstillstånd

    Följande försäljningstillstånd har utvidgats i Eftastaterna i EES mellan den 1 januari och 30 juni 2012:

    EU-nummer

    Produkt

    Land

    Datum för godkännande

    EU/1/00/141/002

    Myocet

    Liechtenstein

    30.4.2012

    EU/1/02/222/05

    Tamiflu

    Island

    6.2.2012

    EU/1/03/262/009–010

    Emend

    Norge

    5.1.2012

    EU/1/03/262/009–010

    Emend

    Island

    3.2.2012

    EU/1/03/271/007–010

    Advate

    Norge

    23.1.2012

    EU/1/03/271/007–010

    Advate

    Island

    17.1.2012

    EU/1/05/318/003

    Revatio

    Norge

    13.4.2012

    EU/1/05/318/003

    Revatio

    Island

    17.4.2012

    EU/1/05/318/003

    Revatio

    Liechtenstein

    30.4.2012

    EU/1/06/339/003

    Preotact

    Liechtenstein

    30.6.2012

    EU/1/08/465/021

    Clopidogrel Zentiva

    Liechtenstein

    30.6.2012

    EU/1/08/468/002

    INTELENCE

    Island

    3.1.2012

    EU/1/08/470/018–019

    Vimpat

    Norge

    14.3.2012

    EU/1/08/470/018–019

    Vimpat

    Island

    14.3.2012

    EU/1/08/470/018–019

    Vimpat

    Liechtenstein

    30.4.2012

    EU/1/08/472/011–021

    Xarelto

    Norge

    4.1.2012

    EU/1/08/475/035–060

    Olanzapin Mylan

    Liechtenstein

    29.2.2012

    EU/1/09/536/003–004

    Topotecan Actavis

    Liechtenstein

    30.4.2012

    EU/1/09/551/013–027

    Vizarsin

    Island

    7.6.2012

    EU/1/09/551/013–027

    Vizarsin

    Liechtenstein

    30.6.2012

    EU/1/09/571/002

    Pandemiskt influensavaccin H5N1 Baxter

    Liechtenstein

    30.4.2012

    EU/1/11/667/004

    Esbriet

    Liechtenstein

    30.4.2012

    EU/1/11/699/003–004

    Fampyra

    Liechtenstein

    30.4.2012

    EU/1/11/701/029–032

    Levetiracetam Teva

    Liechtenstein

    30.6.2012

    EU/1/11/703/003

    Xgeva

    Liechtenstein

    29.2.2012

    EU/1/11/704/002

    Victrelis

    Liechtenstein

    30.4.2012

    EU/1/11/720/002

    Incivo

    Liechtenstein

    30.6.2012

    EU/1/97/044/009

    Tasmar

    Liechtenstein

    30.4.2012

    EU/2/07/078/015–017

    Rheumocam

    Norge

    13.2.2012

    EU/2/07/078/015–017

    Rheumocam

    Island

    7.2.2012

    EU/2/07/078/015–017

    Rheumocam

    Liechtenstein

    29.2.2012

    EU/2/08/085/002–006

    Easotic

    Liechtenstein

    30.4.2012

    EU/2/08/090/027

    Loxicom

    Liechtenstein

    30.6.2012

    EU/2/10/114/003

    Hiprabovis IBR Marker Live

    Liechtenstein

    29.2.2012

    EU/2/97/004/049

    Metacam

    Liechtenstein

    29.2.2012


    BILAGA IV

    Förteckning över återkallade försäljningstillstånd

    Följande försäljningstillstånd har återkallats i Eftastaterna i EES mellan den 1 januari och 30 juni 2012:

    EU-nummer

    Produkt

    Land

    Datum för återkallelse

    EU/1/02/255/001–002

    Xigris

    Island

    25.6.2012

    EU/1/04/272/001–002

    PhotoBarr

    Norge

    24.5.2012

    EU/1/04/272/001–002

    Photobarr

    Island

    20.5.2012

    EU/1/04/272/001–002

    PhotoBarr

    Liechtenstein

    30.6.2012

    EU/1/06/335/001

    Valtropin

    Island

    5.6.2012

    EU/1/06/335/001

    Valtropin

    Liechtenstein

    30.6.2012

    EU/1/06/351/001–003

    Livensa

    Island

    11.4.2012

    EU/1/06/351/001–003

    Livensa

    Liechtenstein

    30.4.2012

    EU/1/06/352/001–003

    Intrinsa

    Liechtenstein

    30.6.2012

    EU/1/06/352/001–003

    Intrinsa

    Island

    23.6.2012

    EU/1/09/534/001–007

    Clopidogrel Hexal

    Island

    2.3.2012

    EU/1/09/534/001–007

    Clopidgrel Hexal

    Liechtenstein

    29.2.2012

    EU/1/09/548/001–007

    Clopidogrel Acino Pharma GmbH

    Island

    2.3.2012

    EU/1/09/548/001–007

    Clopidgrel Acino Pharma GmbH

    Liechtenstein

    29.2.2012

    EU/1/09/549/001–007

    Clopidogrel Acino Pharma

    Island

    2.3.2012

    EU/1/09/549/001–007

    Clopidogrel Acino Pharma

    Liechtenstein

    29.2.2012

    EU/1/10/630/001–002

    Docefrez

    Island

    20.6.2012

    EU/1/10/630/001–002

    Docefrez

    Liechtenstein

    30.6.2012

    EU/1/97/035/003–004

    Refludan

    Island

    24.5.2012

    EU/1/97/035/001–004

    Refludan

    Norge

    6.6.2012

    EU/1/97/035/001–004

    Refludan

    Liechtenstein

    30.6.2012

    EU/2/00/028/002–008

    Zubrin

    Island

    17.4.2012

    EU/2/00/028/002–008

    Zubrin

    Liechtenstein

    30.4.2012

    EU/2/03/040/001–002

    Gonazon

    Norge

    2.4.2012

    EU/2/03/040/001–002

    Gonazon

    Island

    17.4.2012

    EU/2/03/040/001–002

    Gonazon

    Liechtenstein

    30.4.2012

    EU/2/06/060/001–002

    Poulvac FluFend H5N3 RG

    Liechtenstein

    30.6.2012


    BILAGA V

    Förteckning över upphävda försäljningstillstånd

    Följande försäljningstillstånd har upphävts i Eftastaterna i EES mellan den 1 januari och 30 juni 2012:

    EU-nummer

    Produkt

    Land

    Datum för upphävande

    EU/1/06/361/001–002

    Luminity

    Island

    20.6.2012

    EU/1/06/361/001–002

    Luminity

    Liechtenstein

    30.6.2012

    EU/1/97/037/001

    Vistide

    Liechtenstein

    29.2.2012

    EU/1/11/705/001

    Vibativ

    Island

    27.6.2012


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