ISSN 1977-091X |
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Official Journal of the European Union |
C 144 |
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English edition |
Information and Notices |
Volume 65 |
Contents |
page |
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IV Notices |
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NOTICES FROM EUROPEAN UNION INSTITUTIONS, BODIES, OFFICES AND AGENCIES |
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European Commission |
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2022/C 144/01 |
EN |
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IV Notices
NOTICES FROM EUROPEAN UNION INSTITUTIONS, BODIES, OFFICES AND AGENCIES
European Commission
31.3.2022 |
EN |
Official Journal of the European Union |
C 144/1 |
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 February 2022 to 28 February 2022
(Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council (1))
(2022/C 144/01)
— Issuing of a marketing authorisation (Article 13 of Regulation (EC) No 726/2004 of the European Parliament and of the Council): Accepted
Date of the decision |
Name of the medicinal product |
INN (International Non-Proprietary Name) |
Holder of the marketing authorisation |
Number of the entry in the Community Register |
Pharmaceutical form |
ATC code (Anatomical Therapeutic Chemical Code) |
Date of notification |
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14.2.2022 |
Apexxnar |
pneumococcal polysaccharide conjugate vaccine (20-valent, adsorbed) |
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EU/1/21/1612 |
Suspension for injection |
J07AL02 |
15.2.2022 |
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14.2.2022 |
Ngenla |
somatrogon |
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EU/1/21/1617 |
Solution for injection |
Pending |
15.2.2022 |
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14.2.2022 |
OKEDI |
risperidone |
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EU/1/21/1621 |
Powder and solvent for prolonged-release suspension for injection |
N05AX08 |
15.2.2022 |
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14.2.2022 |
Oxbryta |
voxelotor |
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EU/1/21/1622 |
Film-coated tablet |
B06AX |
15.2.2022 |
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14.2.2022 |
Saphnelo |
anifrolumab |
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EU/1/21/1623 |
Concentrate for solution for infusion |
L04AA51 |
15.2.2022 |
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16.2.2022 |
Kerendia |
finerenone |
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EU/1/21/1616 |
Film-coated tablet |
C03DA05 |
17.2.2022 |
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16.2.2022 |
Sapropterin Dipharma |
sapropterin |
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EU/1/21/1620 |
Powder for oral solution Soluble tablet |
A16AX07 |
17.2.2022 |
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16.2.2022 |
Sitagliptin/Metformin hydrochloride Mylan |
sitagliptin/metformin hydrochloride |
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EU/1/21/1619 |
Film-coated tablet |
A10BD07 |
21.2.2022 |
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16.2.2022 |
Tepmetko |
tepotinib |
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EU/1/21/1596 |
Film-coated tablet |
L01EX21 |
17.2.2022 |
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21.2.2022 |
Ontilyv |
opicapone |
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EU/1/21/1578 |
Capsule, hard |
N04BX04 |
22.2.2022 |
— Modification of a marketing authorisation (Article 13 of Regulation (EC) No 726/2004 of the European Parliament and of the Council): Accepted
Date of the decision |
Name of the medicinal product |
Holder of the marketing authorisation |
Number of the entry in the Community Register |
Date of notification |
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2.2.2022 |
Vaxzevria |
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EU/1/21/1529 |
2.2.2022 |
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3.2.2022 |
Clopidogrel Viatris |
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EU/1/09/568 |
7.2.2022 |
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3.2.2022 |
DaTSCAN |
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EU/1/00/135 |
9.2.2022 |
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3.2.2022 |
Edarbi |
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EU/1/11/734 |
8.2.2022 |
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3.2.2022 |
Efavirenz/Emtricitabine/Tenofovir disoproxil Krka |
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EU/1/17/1263 |
9.2.2022 |
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3.2.2022 |
Nyxoid |
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EU/1/17/1238 |
7.2.2022 |
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3.2.2022 |
Pregabalin Zentiva |
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EU/1/15/1021 |
8.2.2022 |
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3.2.2022 |
Vivanza |
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EU/1/03/249 |
7.2.2022 |
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3.2.2022 |
Voriconazole Accord |
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EU/1/13/835 |
4.2.2022 |
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3.2.2022 |
Xigduo |
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EU/1/13/900 |
4.2.2022 |
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4.2.2022 |
Cialis |
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EU/1/02/237 |
8.2.2022 |
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4.2.2022 |
Comirnaty |
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EU/1/20/1528 |
4.2.2022 |
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4.2.2022 |
Ebixa |
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EU/1/02/219 |
8.2.2022 |
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4.2.2022 |
Ebymect |
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EU/1/15/1051 |
7.2.2022 |
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4.2.2022 |
Entacapone Teva |
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EU/1/10/665 |
8.2.2022 |
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4.2.2022 |
HyQvia |
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EU/1/13/840 |
7.2.2022 |
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4.2.2022 |
Iressa |
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EU/1/09/526 |
7.2.2022 |
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4.2.2022 |
Neupro |
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EU/1/05/331 |
9.2.2022 |
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4.2.2022 |
Noxafil |
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EU/1/05/320 |
8.2.2022 |
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4.2.2022 |
Plegridy |
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EU/1/14/934 |
9.2.2022 |
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4.2.2022 |
Revolade |
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EU/1/10/612 |
7.2.2022 |
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4.2.2022 |
Roclanda |
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EU/1/20/1502 |
10.2.2022 |
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4.2.2022 |
Sivextro |
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EU/1/15/991 |
8.2.2022 |
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4.2.2022 |
Temozolomide Accord |
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EU/1/10/615 |
9.2.2022 |
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4.2.2022 |
Vantobra |
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EU/1/18/1350 |
10.2.2022 |
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4.2.2022 |
Yellox |
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EU/1/11/692 |
14.2.2022 |
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4.2.2022 |
Zoledronic acid Hospira |
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EU/1/12/800 |
7.2.2022 |
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10.2.2022 |
Ameluz |
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EU/1/11/740 |
15.2.2022 |
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10.2.2022 |
Axumin |
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EU/1/17/1186 |
15.2.2022 |
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10.2.2022 |
Cotellic |
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EU/1/15/1048 |
14.2.2022 |
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10.2.2022 |
Nityr |
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EU/1/18/1290 |
15.2.2022 |
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10.2.2022 |
Wakix |
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EU/1/15/1068 |
3.3.2022 |
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14.2.2022 |
Cubicin |
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EU/1/05/328 |
18.2.2022 |
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14.2.2022 |
Incruse Ellipta |
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EU/1/14/922 |
4.3.2022 |
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14.2.2022 |
Ivabradine Accord |
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EU/1/17/1190 |
15.2.2022 |
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14.2.2022 |
Spikevax |
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EU/1/20/1507 |
16.2.2022 |
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14.2.2022 |
Waylivra |
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EU/1/19/1360 |
21.2.2022 |
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14.2.2022 |
Xromi |
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EU/1/19/1366 |
17.2.2022 |
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16.2.2022 |
AMGLIDIA |
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EU/1/18/1279 |
16.2.2022 |
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16.2.2022 |
Besponsa |
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EU/1/17/1200 |
17.2.2022 |
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16.2.2022 |
CellCept |
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EU/1/96/005 |
17.2.2022 |
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16.2.2022 |
Deltyba |
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EU/1/13/875 |
17.2.2022 |
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16.2.2022 |
Eliquis |
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EU/1/11/691 |
17.2.2022 |
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16.2.2022 |
ellaOne |
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EU/1/09/522 |
23.2.2022 |
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16.2.2022 |
Envarsus |
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EU/1/14/935 |
21.2.2022 |
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16.2.2022 |
Febuxostat Mylan |
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EU/1/17/1194 |
17.2.2022 |
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16.2.2022 |
JEMPERLI |
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EU/1/21/1538 |
17.2.2022 |
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16.2.2022 |
Laventair Ellipta |
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EU/1/14/899 |
4.3.2022 |
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16.2.2022 |
Mayzent |
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EU/1/19/1414 |
17.2.2022 |
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16.2.2022 |
Modigraf |
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EU/1/09/523 |
17.2.2022 |
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16.2.2022 |
Myclausen |
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EU/1/10/647 |
17.2.2022 |
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16.2.2022 |
Pemazyre |
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EU/1/21/1535 |
21.2.2022 |
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16.2.2022 |
Pregabalin Sandoz |
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EU/1/15/1011 |
21.2.2022 |
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16.2.2022 |
Riximyo |
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EU/1/17/1184 |
17.2.2022 |
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16.2.2022 |
Temybric Ellipta |
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EU/1/19/1378 |
4.3.2022 |
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16.2.2022 |
Yuflyma |
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EU/1/20/1513 |
2.3.2022 |
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16.2.2022 |
Zykadia |
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EU/1/15/999 |
17.2.2022 |
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17.2.2022 |
Advagraf |
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EU/1/07/387 |
21.2.2022 |
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17.2.2022 |
Avonex |
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EU/1/97/033 |
23.2.2022 |
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17.2.2022 |
Mycophenolate mofetil Teva |
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EU/1/07/439 |
18.2.2022 |
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17.2.2022 |
Myfenax |
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EU/1/07/438 |
21.2.2022 |
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17.2.2022 |
Nexium Control |
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EU/1/13/860 |
24.2.2022 |
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18.2.2022 |
Tarceva |
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EU/1/05/311 |
21.2.2022 |
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18.2.2022 |
Zelboraf |
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EU/1/12/751 |
21.2.2022 |
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21.2.2022 |
Clopidogrel Taw Pharma |
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EU/1/09/559 |
22.2.2022 |
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21.2.2022 |
Jardiance |
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EU/1/14/930 |
25.2.2022 |
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21.2.2022 |
Ogivri |
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EU/1/18/1341 |
23.2.2022 |
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21.2.2022 |
Refixia |
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EU/1/17/1193 |
24.2.2022 |
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21.2.2022 |
Skilarence |
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EU/1/17/1201 |
23.2.2022 |
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23.2.2022 |
Tecentriq |
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EU/1/17/1220 |
25.2.2022 |
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24.2.2022 |
ADVATE |
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EU/1/03/271 |
28.2.2022 |
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24.2.2022 |
Bortezomib Hospira |
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EU/1/16/1114 |
25.2.2022 |
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24.2.2022 |
Briviact |
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EU/1/15/1073 |
25.2.2022 |
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24.2.2022 |
Irbesartan Teva |
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EU/1/09/576 |
28.2.2022 |
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24.2.2022 |
JEVTANA |
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EU/1/11/676 |
28.2.2022 |
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24.2.2022 |
Lacosamide UCB |
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EU/1/19/1383 |
25.2.2022 |
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24.2.2022 |
Rixathon |
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EU/1/17/1185 |
25.2.2022 |
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24.2.2022 |
Senshio |
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EU/1/14/978 |
25.2.2022 |
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28.2.2022 |
Comirnaty |
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EU/1/20/1528 |
28.2.2022 |
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28.2.2022 |
Imfinzi |
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EU/1/18/1322 |
2.3.2022 |
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28.2.2022 |
Nimenrix |
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EU/1/12/767 |
1.3.2022 |
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28.2.2022 |
Retsevmo |
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EU/1/20/1527 |
2.3.2022 |
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28.2.2022 |
Xagrid |
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EU/1/04/295 |
1.3.2022 |
— Withdrawal of a marketing authorisation (Article 13 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)
Date of the decision |
Name of the medicinal product |
Holder of the marketing authorisation |
Number of the entry in the Community Register |
Date of notification |
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3.2.2022 |
Vivanza |
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EU/1/03/249 |
7.2.2022 |
— Modification of a marketing authorisation (Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council): Accepted
Date of the decision |
Name of the medicinal product |
Holder of the marketing authorisation |
Number of the entry in the Community Register |
Date of notification |
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1.2.2022 |
Bravecto |
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EU/2/13/158 |
3.2.2022 |
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1.2.2022 |
Mirataz |
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EU/2/19/247 |
2.2.2022 |
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8.2.2022 |
Exzolt |
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EU/2/17/212 |
9.2.2022 |
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8.2.2022 |
Zulvac 8 Ovis |
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EU/2/09/104 |
9.2.2022 |
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10.2.2022 |
Draxxin |
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EU/2/03/041 |
16.2.2022 |
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10.2.2022 |
Nobilis IB 4-91 |
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EU/2/98/006 |
14.2.2022 |
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10.2.2022 |
Onsior |
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EU/2/08/089 |
11.2.2022 |
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28.2.2022 |
Innovax-ND-IBD |
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EU/2/17/213 |
2.3.2022 |
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28.2.2022 |
Innovax-ND-ILT |
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EU/2/20/256 |
2.3.2022 |
Anyone wishing to consult the public assessment report on the medicinal products in question and the decisions relating thereto is invited to contact:
European Medicines Agency |
Domenico Scarlattilaan 6 |
1083 HS Amsterdam |
NETHERLANDS |