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Document E2014G1106(01)

    Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2013

    OJ C 391, 6.11.2014, p. 3–14 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    6.11.2014   

    EN

    Official Journal of the European Union

    C 391/3


    Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2013

    2014/C 391/03

    Subcommitee I on the free movement of goods

    To be noted by the EEA Joint Committee

    With reference to EEA Joint Committee Decision No 74/1999 of 28 May 1999, the EEA Joint Committee is invited to note the following lists concerning marketing authorisations for medicinal products for the period 1 January - 30 June 2013, at their meeting on 4 April 2014:

    Annex I

    List of new marketing authorisations

    Annex II

    List of renewed marketing authorisations

    Annex III

    List of extended marketing authorisations

    Annex IV

    List of withdrawn marketing authorisations

    Annex V

    List of suspended marketing authorisations


    ANNEX I

    List of new marketing authorisations

    The following marketing authorisations have been granted in the EEA EFTA States during the period 1 January-30 June 2013:

    EU-Number

    Product

    Country

    Date of authorisation

    EU/1/12/788/001-006

    Seebri Breezhaler

    Liechtenstein

    30.4.2013

    EU/1/12/789/001-006

    Enurev Breezhaler

    Liechtenstein

    30.4.2013

    EU/1/12/790/001-006

    Tovanor Breezhaler

    Liechtenstein

    30.4.2013

    EU/1/12/791/001

    Glybera

    Liechtenstein

    30.4.2013

    EU/1/12/795/001-010

    Forxiga

    Liechtenstein

    30.4.2013

    EU/1/12/797/001-002

    Eylea

    Liechtenstein

    30.4.2013

    EU/1/12/803/001-002

    NexoBrid

    Liechtenstein

    30.4.2013

    EU/1/12/803/001-002

    NexoBrid

    Iceland

    14.1.2013

    EU/1/12/803/001-002

    NexoBrid

    Norway

    11.1.2013

    EU/1/12/804/001-016

    BindRen

    Liechtenstein

    30.4.2013

    EU/1/12/804/001-016

    BindRen

    Iceland

    8.2.2013

    EU/1/12/804/001-016

    BindRen

    Norway

    27.2.2013

    EU/1/12/805

    Amyvid

    Liechtenstein

    28.2.2013

    EU/1/12/805/001-004

    AMYViD

    Iceland

    6.2.2013

    EU/1/12/805/001-004

    AMYViD

    Norway

    4.2.2013

    EU/1/12/806/001-005

    Ryzodeg

    Liechtenstein

    28.2.2013

    EU/1/12/806/001-005

    Ryzodeg

    Iceland

    20.2.2013

    EU/1/12/806/001-005

    Ryzodeg

    Norway

    12.2.2013

    EU/1/12/807/001-009

    Tresiba

    Liechtenstein

    28.2.2013

    EU/1/12/807/001-009

    Tresiba

    Iceland

    20.2.2013

    EU/1/12/807/001-009

    Tresiba

    Norway

    12.2.2013

    EU/1/12/808/001-040

    Imatinib Teva

    Liechtenstein

    28.2.2013

    EU/1/12/808/001-040

    Imatinib Teva

    Iceland

    5.2.2013

    EU/1/12/808/001-040

    Imatinib Teva

    Norway

    22.1.2013

    EU/1/12/809/001-014

    Betmiga

    Liechtenstein

    28.2.2013

    EU/1/12/809/001-014

    Betmiga

    Iceland

    10.1.2013

    EU/1/12/809/001-014

    Betmiga

    Norway

    17.1.2013

    EU/1/12/810

    Krystexxa

    Liechtenstein

    30.4.2013

    EU/1/12/810/001

    Krystexxa

    Iceland

    14.1.2013

    EU/1/12/810/001

    Krystexxa

    Norway

    25.1.2013

    EU/1/12/811/001-005

    Lyxumia

    Iceland

    12.2.2013

    EU/1/12/811/001-005

    Lyxumia

    Norway

    12.2.2013

    EU/1/12/812

    Bexsero

    Liechtenstein

    28.2.2013

    EU/1/12/812/001-004

    Bexsero

    Iceland

    14.2.2013

    EU/1/12/812/001-004

    Bexsero

    Norway

    4.2.2013

    EU/1/12/814

    Zaltrap

    Liechtenstein

    28.2.2013

    EU/1/12/814/001-003

    Zaltrap

    Iceland

    12.2.2013

    EU/1/12/814/001-003

    Zaltrap

    Norway

    27.2.2013

    EU/1/12/815/001-005

    Selincro

    Liechtenstein

    30.4.2013

    EU/1/12/815/001-005

    Selincro

    Iceland

    19.3.2013

    EU/1/12/815/001-005

    Selincro

    Norway

    11.3.2013

    EU/1/13/813/001

    Perjeta

    Liechtenstein

    30.4.2013

    EU/1/13/813/001

    Perjeta

    Iceland

    20.3.2013

    EU/1/13/813/001

    Perjeta

    Norway

    9.4.2013

    EU/1/13/817/001-041

    Actelsar HCT

    Iceland

    21.3.2013

    EU/1/13/817/001-041

    Actelsar HCT

    Norway

    22.4.2013

    EU/1/13/818/001-004

    Bosulif

    Iceland

    15.4.2013

    EU/1/13/818/001-004

    Bosulif

    Norway

    30.4.2013

    EU/1/13/819/001

    JETREA

    Liechtenstein

    30.4.2013

    EU/1/13/819/001

    JETREA

    Iceland

    11.4.2013

    EU/1/13/819/001

    JETREA

    Norway

    22.3.2013

    EU/1/13/820/001-026

    Maruxa

    Liechtenstein

    30.6.2013

    EU/1/13/820/001-026

    Maruxa

    Norway

    24.5.2013

    EU/1/13/821/001-030

    Tolucombi

    Liechtenstein

    30.4.2013

    EU/1/13/821/001-030

    Tolucombi

    Iceland

    21.3.2013

    EU/1/13/821/001-030

    Tolucombi

    Norway

    22.3.2013

    EU/1/13/823/001-002

    Adasuve

    Norway

    12.3.2013

    EU/1/13/823/001-002

    Adasuve

    Liechtenstein

    30.4.2013

    EU/1/13/823/001-002

    Adasuve

    Iceland

    18.3.2013

    EU/1/13/824

    Nemdatine

    Liechtenstein

    30.4.2013

    EU/1/13/824/001-020

    Nemdatine

    Iceland

    21.5.2013

    EU/1/13/824/001-020

    Nemdatine

    Norway

    3.5.2013

    EU/1/13/825

    Imatinib Actavis

    Liechtenstein

    30.6.2013

    EU/1/13/825/001-018

    Imatinib Actavis

    Iceland

    16.5.2013

    EU/1/13/825/001-018

    Imatinib Actavis

    Norway

    20.6.2013

    EU/1/13/826

    Memantine LEK

    Liechtenstein

    30.4.2013

    EU/1/13/826/001-011

    Memantine LEK

    Iceland

    21.5.2013

    EU/1/13/826/001-011

    Memantine LEK

    Norway

    3.5.2013

    EU/1/13/827

    Memantine Mylan

    Liechtenstein

    30.4.2013

    EU/1/13/827/001-036

    Memantine Mylan

    Iceland

    21.5.2013

    EU/1/13/827/001-036

    Memantine Mylan

    Norway

    3.5.2013

    EU/1/13/828

    Hexacima

    Liechtenstein

    30.4.2013

    EU/1/13/828/001-007

    Hexacima

    Iceland

    17.5.2013

    EU/1/13/828/001-007

    Hexacima

    Norway

    15.5.2013

    EU/1/13/829

    Hexyon

    Liechtenstein

    30.4.2013

    EU/1/13/829/001-007

    Hexyon

    Iceland

    17.5.2013

    EU/1/13/829/001-007

    Hexyon

    Norway

    15.5.2013

    EU/1/13/830/001-002

    Stribild

    Iceland

    19.6.2013

    EU/1/13/830/001-002

    Stribild

    Norway

    24.5.2013

    EU/1/13/835/001-018

    Voriconazole Accord

    Iceland

    31.5.2013

    EU/1/13/835/001-018

    Voriconazole Accord

    Norway

    31.5.2013

    EU/1/13/836

    Memantine ratiopharm

    Liechtenstein

    30.6.2013

    EU/1/13/836/001-023

    Memantine ratiopharm

    Norway

    25.6.2013

    EU/1/13/840/001-005

    HyQvia

    Iceland

    27.5.2013

    EU/1/13/840/001-005

    HyQvia

    Norway

    3.6.2013

    EU/2/12/142/001-006

    Cardalis

    Norway

    20.6.2013

    EU/2/12/144/001-004

    Contacera

    Liechtenstein

    28.2.2013

    EU/2/12/144/001-004

    Contacera

    Iceland

    3.1.2013

    EU/2/12/144/001-004

    Contacera

    Norway

    17.1.2013

    EU/2/12/145/001-003

    Kexxtone

    Liechtenstein

    30.4.2013

    EU/2/12/145/001-003

    Kexxtone

    Iceland

    27.2.2013

    EU/2/12/145/001-003

    Kexxtone

    Norway

    8.3.2013

    EU/2/12/146/001

    Semintra

    Liechtenstein

    30.4.2013

    EU/2/12/146/001

    Semintra

    Iceland

    12.3.2013

    EU/2/12/146/001

    Semintra

    Norway

    5.4.2013

    EU/2/12/147/001-004

    Pexion

    Liechtenstein

    30.4.2013

    EU/2/12/147/001-004

    Pexion

    Iceland

    19.3.2013

    EU/2/12/147/001-004

    Pexion

    Norway

    8.3.2013

    EU/2/13/148

    Meloxidolor

    Liechtenstein

    30.6.2013

    EU/2/13/148/001-007

    Meloxidolor

    Iceland

    21.5.2013

    EU/2/13/148/001-007

    Meloxidolor

    Norway

    22.4.2013

    EU/2/13/149

    ECOPORC SHIGA

    Liechtenstein

    30.4.2013

    EU/2/13/149/001-002

    ECOPORC SHIGA

    Iceland

    15.5.2013

    EU/2/13/149/001-002

    ECOPORC SHIGA

    Norway

    13.5.2013

    EU/2/13/150

    Oncept IL-2

    Liechtenstein

    30.6.2013

    EU/2/13/151/001-003

    Equilis West Nile

    Iceland

    27.6.2013


    ANNEX II

    List of renewed marketing authorisations

    The following marketing authorisations have been renewed in the EEA EFTA States during the period 1 January-30 June 2013:

    EU-Number

    Product

    Country

    Date of authorisation

    EU/1/03/247

    Forsteo

    Liechtenstein

    30.4.2013

    EU/1/03/247/001-002

    Forsteo

    Iceland

    19.2.2013

    EU/1/03/247/001-002

    Forsteo

    Norway

    6.3.2013

    EU/1/07/423

    Vectibix

    Liechtenstein

    30.4.2013

    EU/1/07/423/001-003

    Vectibix

    Iceland

    5.2.2013

    EU/1/07/423/001-003

    Vectibix

    Norway

    12.2.2013

    EU/1/07/428/001

    Abraxane

    Liechtenstein

    30.4.2013

    EU/1/07/428/001

    Abraxane

    Iceland

    5.2.2013

    EU/1/07/428/001

    Abraxane

    Norway

    11.2.2013

    EU/1/07/430/001-002

    Atripla

    Liechtenstein

    30.4.2013

    EU/1/07/433/001

    Nevanac

    Iceland

    9.1.2013

    EU/1/07/434

    Avamys

    Liechtenstein

    28.2.2013

    EU/1/07/434/001-003

    Avamys

    Iceland

    11.1.2013

    EU/1/07/434/001-003

    Avamys

    Norway

    14.1.2013

    EU/1/07/435/001-018

    Tesavel

    Liechtenstein

    30.4.2013

    EU/1/07/438/001-006

    Myfenax

    Liechtenstein

    30.4.2013

    EU/1/07/439/001-006

    Mycophenolate mofetil Teva

    Liechtenstein

    30.4.2013

    EU/1/07/440

    Tyverb

    Liechtenstein

    30.4.2013

    EU/1/07/440/001-007

    Tyverb

    Norway

    15.5.2013

    EU/1/08/441

    Effentora

    Liechtenstein

    30.4.2013

    EU/1/08/441/001-010

    Effentora

    Iceland

    20.3.2013

    EU/1/08/441/001-010

    Effentora

    Norway

    12.3.2013

    EU/1/08/442/001-019

    Pradaxa

    Norway

    26.2.2013

    EU/1/08/442/001-019

    Pradaxa

    Liechtenstein

    30.4.2013

    EU/1/08/442/001-019

    Pradaxa

    Iceland

    15.2.2013

    EU/1/08/443/001

    Thalidomide Celgene

    Iceland

    14.1.2013

    EU/1/08/443/001

    Thalidomide Celgene

    Norway

    16.1.2013

    EU/1/08/446/001-006

    Privigen

    Iceland

    22.3.2013

    EU/1/08/446/001-006

    Privigen

    Norway

    21.3.2013

    EU/1/08/447/001-012

    Adenuric

    Norway

    15.1.2013

    EU/1/08/447/001-012

    Adenuric

    Liechtenstein

    30.4.2013

    EU/1/08/447/001-012

    Adenuric

    Iceland

    14.1.2013

    EU/1/08/448/001-002

    Mycamine

    Liechtenstein

    30.4.2013

    EU/1/08/448/001-002

    Mycamine

    Iceland

    24.1.2013

    EU/1/08/448/001-002

    Mycamine

    Norway

    12.2.2013

    EU/1/08/451

    Volibris

    Liechtenstein

    30.4.2013

    EU/1/08/451/001-004

    Volibris

    Iceland

    5.2.2013

    EU/1/08/451/001-004

    Volibris

    Norway

    12.2.2013

    EU/1/08/453

    Prepandrix

    Liechtenstein

    30.4.2013

    EU/1/08/453/002

    Prepandrix

    Iceland

    6.2.2013

    EU/1/08/453/002

    Prepandrix

    Norway

    4.2.2013

    EU/1/08/454/001-002, 005-007

    Extavia

    Iceland

    9.1.2013

    EU/1/08/454/001-002, 005-007

    Extavia

    Liechtenstein

    30.4.2013

    EU/1/08/454/001-002, 005-007

    Extavia

    Norway

    10.1.2013

    EU/1/08/455

    Janumet

    Liechtenstein

    30.4.2013

    EU/1/08/455/001-006

    Janumet

    Norway

    10.4.2013

    EU/1/08/455/001-016

    Janumet

    Iceland

    25.3.2013

    EU/1/08/456

    Velmetia

    Liechtenstein

    30.4.2013

    EU/1/08/456/001-016

    Velmetia

    Iceland

    26.3.2013

    EU/1/08/457

    Efficib

    Liechtenstein

    30.4.2013

    EU/1/08/457/001-016

    Efficib

    Iceland

    26.3.2013

    EU/1/08/461

    Firazyr

    Liechtenstein

    30.4.2013

    EU/1/08/461/001-002

    Firazyr

    Iceland

    11.4.2013

    EU/1/08/461/001-002

    Firazyr

    Norway

    10.4.2013

    EU/1/08/462

    Ranexa

    Liechtenstein

    30.4.2013

    EU/1/08/462/001-002

    Ranexa

    Norway

    9.4.2013

    EU/1/08/462/001-012

    Ranexa

    Iceland

    20.3.2013

    EU/1/08/463

    Relistor

    Liechtenstein

    30.6.2013

    EU/1/08/463/001-011

    Relistor

    Iceland

    21.6.2013

    EU/1/08/463/001-011

    Relistor

    Norway

    26.6.2013

    EU/1/08/465

    Clopidogrel Zentiva

    Liechtenstein

    28.2.2013

    EU/1/08/465/001-021

    Clopidogrel Zentiva

    Iceland

    3.1.2013

    EU/1/08/465/001-021

    Clopidogrel Zentiva

    Norway

    5.2.2013

    EU/1/08/467

    Doribax

    Liechtenstein

    30.6.2013

    EU/1/08/467/001-002

    Doribax

    Iceland

    17.5.2013

    EU/1/08/469

    Oprymea

    Liechtenstein

    30.4.2013

    EU/1/08/469/001-025

    Oprymea

    Iceland

    14.5.2013

    EU/1/08/469/001-025

    Oprymea

    Norway

    24.5.2013

    EU/1/08/472

    Xarelto

    Liechtenstein

    30.6.2013

    EU/1/08/472/001-033

    Xarelto

    Norway

    13.6.2013

    EU/1/08/472/001-033

    Xarelto

    Iceland

    20.6.2013

    EU/1/08/475

    Olanzapine Mylan

    Liechtenstein

    30.6.2013

    EU/1/08/475/001-060

    Olanzapine Mylan

    Iceland

    20.6.2013

    EU/1/08/475/001-060

    Olanzapine Mylan

    Norway

    7.6.2013

    EU/1/08/476

    Adcirca

    Liechtenstein

    30.6.2013

    EU/1/08/476/005-006

    Adcirca

    Iceland

    31.5.2013

    EU/1/08/476/005-006

    Adcirca

    Norway

    4.6.2013

    EU/1/10/625

    Arzerra

    Liechtenstein

    30.4.2013

    EU/1/10/625/001, 003

    Arzerra

    Iceland

    15.3.2013

    EU/1/10/625/001, 003

    Arzerra

    Norway

    9.4.2013

    EU/1/11/749

    Caprelsa

    Liechtenstein

    30.4.2013

    EU/1/11/749/001-002

    Caprelsa

    Iceland

    12.3.2013

    EU/1/11/749/001-002

    Caprelsa

    Norway

    9.4.2013

    EU/1/12/764

    Pixuvri

    Liechtenstein

    30.4.2013

    EU/1/12/764/001

    Pixuvri

    Iceland

    12.4.2013

    EU/1/12/764/001

    Pixuvri

    Norway

    9.4.2013

    EU/1/97/055/001-009

    Viramune

    Liechtenstein

    30.4.2013

    EU/1/97/055/001-009

    Viramune

    Iceland

    14.1.2013

    EU/1/97/055/001-009

    Viramune

    Norway

    22.1.2013

    EU/2/02/032/001-002

    Vaxxitec HVT+IBD

    Norway

    11.6.2013

    EU/2/03/037

    ProteqFlu

    Liechtenstein

    30.4.2013

    EU/2/03/037/005

    ProteqFlu

    Iceland

    21.3.2013

    EU/2/03/037/005

    ProteqFlu

    Norway

    20.6.2013

    EU/2/03/038

    ProteqFlu-Te

    Liechtenstein

    30.4.2013

    EU/2/03/038/005

    ProteqFlu-Te

    Iceland

    21.3.2013

    EU/2/03/038/005

    ProteqFlu-Te

    Norway

    20.6.2013

    EU/2/03/039

    Advocate

    Liechtenstein

    28.2.2013

    EU/2/03/039/001-054

    Advocate

    Iceland

    19.2.2013

    EU/2/03/039/001-054

    Advocate

    Norway

    5.3.2013

    EU/2/07/074/001-006

    Prilactone

    Norway

    11.6.2013

    EU/2/07/077/001-005

    Meloxivet

    Norway

    5.4.2013

    EU/2/07/078

    Rheumocam

    Liechtenstein

    28.2.2013

    EU/2/07/078/001-020

    Rheumocam

    Iceland

    11.1.2013

    EU/2/07/078/001-020

    Rheumocam

    Norway

    21.1.2013

    EU/2/07/079

    Ingelvac CircoFLEX

    Liechtenstein

    30.4.2013

    EU/2/07/079/001-008

    Ingelvac CircoFLEX

    Iceland

    7.2.2013

    EU/2/07/079/001-008

    Ingelvac CircoFLEX

    Norway

    5.3.2013

    EU/2/08/081/001-003

    Posatex

    Iceland

    14.6.2013

    EU/2/08/081/001-003

    Posatex

    Norway

    11.6.2013

    EU/2/08/083/001-005

    Equioxx

    Iceland

    28.6.2013

    EU/2/08/083/001-005

    Equioxx

    Norway

    20.6.2013


    ANNEX III

    List of extended marketing authorisations

    The following marketing authorisations have been extended in the EEA EFTA States during the period 1 January-30 June 2013:

    EU-Number

    Product

    Country

    Date of authorisation

    EU/1/01/200/003-009

    Viread

    Norway

    11.1.2013

    EU/1/02/221/017

    Pegasys

    Iceland

    26.3.2013

    EU/1/02/221/017

    Pegasys

    Norway

    26.3.2013

    EU/1/06/380/006-007

    Prezista

    Liechtenstein

    28.2.2013

    EU/1/06/380/007

    Prezista

    Iceland

    6.2.2013

    EU/1/06/380/007

    Prezista

    Norway

    11.2.2013

    EU/1/07/433/002

    Nevanac

    Norway

    24.5.2013

    EU/1/07/436/003-004

    Isentress

    Iceland

    19.3.2013

    EU/1/07/436/003-004

    Isentress

    Norway

    25.2.2013

    EU/1/08/468/003

    Intelence

    Norway

    17.4.2013

    EU/1/09/538/009-010

    Afinitor

    Iceland

    5.2.2013

    EU/1/09/538/009-010

    Afinitor

    Norway

    16.1.2013

    EU/1/09/576/041-042

    Irbesartan Teva

    Liechtenstein

    28.2.2013

    EU/1/11/690/003-004

    Zoely

    Liechtenstein

    28.2.2013

    EU/1/11/693/017-024

    Rivastigmine Actavis

    Iceland

    17.5.2013

    EU/1/11/693/017-024

    Rivastigmine Actavis

    Norway

    25.6.2013

    EU/1/12/750/002

    Esmya

    Liechtenstein

    28.2.2013

    EU/1/12/770/005

    Docetaxel Kabi

    Liechtenstein

    28.2.2013

    EU/1/98/066/027-030

    Exelon

    Iceland

    7.2.2013

    EU/1/98/066/027-030

    Exelon

    Norway

    12.2.2013

    EU/1/98/077/020-023

    Viagra

    Iceland

    17.5.2013

    EU/1/98/077/020-023

    Viagra

    Norway

    15.5.2013

    EU/100/146/033-037

    Keppra

    Liechtenstein

    28.2.2013

    EU/2/08/090/029-031

    Loxicom

    Iceland

    21.3.2013

    EU/2/08/090/029-031

    Loxicom

    Norway

    6.3.2013

    EU/2/10/115/016-019

    Comfortis

    Iceland

    8.2.2013

    EU/2/10/115/016-019

    Comfortis

    Norway

    14.1.2013

    EU/2/11/134/018-020

    Inflacam

    Norway

    17.1.2013


    ANNEX IV

    List of withdrawn marketing authorisations

    The following marketing authorisations have been withdrawn in the EEA EFTA States during the period 1 January-30 June 2013:

    EU-Number

    Product

    Country

    Date of withdrawal

    EU/1/03/266

    Bondenza

    Liechtenstein

    30.4.2013

    EU/1/03/266/001-006

    Bondenza

    Norway

    12.6.2013

    EU/1/07/409

    Riprazo

    Liechtenstein

    30.4.2013

    EU/1/07/409/001-040

    Riprazo

    Iceland

    27.5.2013

    EU/1/07/409/001-040

    Riprazo

    Norway

    14.3.2013

    EU/1/08/458/001-014

    Trevaclyn

    Iceland

    15.5.2013

    EU/1/08/458/001-014

    Trevaclyn

    Norway

    23.4.2013

    EU/1/08/459/001-014

    Tredaptive

    Iceland

    15.5.2013

    EU/1/08/459/001-014

    Tredaptive

    Norway

    23.4.2013

    EU/1/08/460/001-014

    Pelzont

    Iceland

    15.5.2013

    EU/1/08/460/001-014

    Pelzont

    Norway

    23.4.2013

    EU/1/08/474/001-003

    Alisade

    Iceland

    27.6.2013

    EU/1/09/582/001

    Rilonacept Regeneron

    Liechtenstein

    28.2.2013

    EU/1/09/582/001

    Rilonacept Regeneron

    Norway

    8.2.2013

    EU/1/10/656/001-006

    Possia

    Iceland

    15.4.2013

    EU/1/10/656/001-006

    Possia

    Norway

    12.6.2013

    EU/1/11/683/001-080

    Sprimeo HCT

    Norway

    21.3.2013

    EU/1/12/754/001-021

    Sepioglin

    Norway

    20.6.2013

    EU/1/97/040/001-002

    Teslascan

    Liechtenstein

    28.2.2013

    EU/2/04/046

    Nobivac Piro

    Liechtenstein

    30.6.2013

    EU/2/04/046/001-003

    Nobivac Piro

    Iceland

    3.6.2013

    EU/2/04/046/001-003

    Nobivac Piro

    Norway

    22.5.2013


    ANNEX V

    List of suspended marketing authorisations

    The following marketing authorisations have been suspended in the EEA EFTA States during the period 1 January-30 June 2013:

    EU-Number

    Product

    Country

    Date of suspension

    EU/1/09/509/001-004

    Ribavirin Teva

    Norway

    3.1.2013

    EU/1/09/527/001-006

    Ribavirin Teva Pharma BV

    Norway

    3.1.2013


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