1 September 2017 EMA/580033/2017 Human Medicines Evaluation Division

List of nationally authorised medicinal products

Active substance: sertindole

Procedure no.: PSUSA/00002695/201701

30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5525 Send a question via our website www.ema.europa.eu/contact

An agency of the European Union

© European Medicines Agency, 2017. Reproduction is authorised provided the source is acknowledged.

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 12 mg

not available

68/0516/97-S

H. LUNDBECK A/S

SK

Serdolect 12 mg

not available

97-0298

H. LUNDBECK A/S

LV

UK/H/0141/003

61.584

H. LUNDBECK A/S

ES

UK/H/0141/003

PL 13761/0003

H. LUNDBECK A/S

UK

UK/H/0141/003

96-0273

H. LUNDBECK A/S

NO

not available

UP/I-530-09/12-02/51

LUNDBECK CROATIA D.O.O.

HR

UK/H/0141/003

RVG 20612

H. LUNDBECK A/S

NL

not available

OGYI-T-5605/02

H. LUNDBECK A/S

HU

UK/H/0141/003

1-21727

H. LUNDBECK A/S

AT

UK/H/0141/003

IS/1/02/026/03

H. LUNDBECK A/S

IS

apvalkotas tabletes Serdolect 12 mg comprimidos recubiertos con película Serdolect 12 mg filmcoated tablets Serdolect 12 mg filmdrasjerte tabletter Serdolect 12 mg filmom obložene tablete Serdolect 12 mg filmomhulde tabletten Serdolect 12 mg filmtabletta Serdolect 12 mgFilmtabletten Serdolect 12 mg filmuhúðaðar töflur

List of nationally authorised medicinal products EMA/580033/2017

Page 2/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

SERDOLECT 12 mg

not available

68/672/96-B/C

H. LUNDBECK A/S

CZ

UK/H/0141/003

12402

H. LUNDBECK A/S

FI

UK/H/0141/003

90515/24-11-2016

LUNDBECK HELLAS, GR

GR

Serdolect 16 mg

not available

68/0516/97-S

H. LUNDBECK A/S

SK

Serdolect 16 mg

not available

97-0299

H. LUNDBECK A/S

LV

UK/H/0141/004

BE285591

H. LUNDBECK A/S

BE

UK/H/0141/04

BE434393

H. LUNDBECK A/S

BE

UK/H/0141/004

BE184265

H. LUNDBECK A/S

BE

UK/H/0141/004

61.585

H. LUNDBECK A/S

ES

potahované tablety Serdolect 12 mg tabletti, kalvopäällysteinen Serdolect 12 mg επικαλυμμένα με λεπτό υμένιο δισκία

apvalkotas tabletes Serdolect 16 mg comprimés pelliculés Serdolect 16 mg comprimés pelliculés Serdolect 16 mg comprimés pelliculés Serdolect 16 mg comprimidos recubiertos con película

List of nationally authorised medicinal products EMA/580033/2017

Page 3/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 16 mg film-

UK/H/0141/004

PL 13761/0004

H. LUNDBECK A/S

UK

UK/H/0141/004

96-0274

H. LUNDBECK A/S

NO

UK/H/0141/004

BE285591

H. LUNDBECK A/S

BE

UK/H/0141/004

BE434393

H. LUNDBECK A/S

BE

UK/H/0141/004

RVG 20613

H. LUNDBECK A/S

NL

not available

OGYI-T-5605/03

H. LUNDBECK A/S

HU

UK/H/0141/004

1-21728

H. LUNDBECK A/S

AT

UK/H/0141/004

IS/1/02/026/04

H. LUNDBECK A/S

IS

not available

68/672/96-C/C

H. LUNDBECK A/S

CZ

coated tablets Serdolect 16 mg filmdrasjerte tabletter Serdolect 16 mg filmomhulde tabletten Serdolect 16 mg filmomhulde tabletten Serdolect 16 mg filmomhulde tabletten Serdolect 16 mg filmtabletta Serdolect 16 mgFilmtabletten Serdolect 16 mg filmuhúðaðar töflur SERDOLECT 16 mg potahované tablety

List of nationally authorised medicinal products EMA/580033/2017

Page 4/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 16 mg tabletti,

UK/H/0141/004

12403

H. LUNDBECK A/S

FI

UK/H/0141/004

90516/24-11-2016

LUNDBECK HELLAS, GR

GR

not available

7721/2015/01-02

H. LUNDBECK A/S

RO

UK/H/0141/004

BE184265

H. LUNDBECK A/S

BE

Serdolect 20 mg

not available

68/0516/97-S

H. LUNDBECK A/S

SK

Serdolect 20 mg

not available

97-0300

H. LUNDBECK A/S

LV

UK/H/0141/005

61.586

H. LUNDBECK A/S

ES

UK/H/0141/005

PL 13761/0005

H. LUNDBECK A/S

UK

UK/H/0141/005

96-0275

H. LUNDBECK A/S

NO

kalvopäällysteinen Serdolect 16 mg επικαλυμμένα με λεπτό υμένιο δισκία Serdolect 16 mg, comprimate filmate Serdolect 16 mg, filmomhulde tabletten

apvalkotas tabletes Serdolect 20 mg comprimidos recubiertos con película Serdolect 20 mg filmcoated tablets Serdolect 20 mg filmdrasjerte tabletter

List of nationally authorised medicinal products EMA/580033/2017

Page 5/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 20 mg

UK/H/0141/005

RVG 20614

H. LUNDBECK A/S

NL

not available

OGYI-T-5605/04

H. LUNDBECK A/S

HU

UK/H/0141/005

1-21729

H. LUNDBECK A/S

AT

UK/H/0141/005

IS/1/02/026/05

H. LUNDBECK A/S

IS

not available

68/672/96-D/C

H. LUNDBECK A/S

CZ

UK/H/0141/005

12404

H. LUNDBECK A/S

FI

UK/H/0141/005

90517/24-11-2016

LUNDBECK HELLAS, GR

GR

Serdolect 4 mg

not available

68/0516/97-S

H. LUNDBECK A/S

SK

Serdolect 4 mg

not available

97-0296

H. LUNDBECK A/S

LV

filmomhulde tabletten Serdolect 20 mg filmtabletta Serdolect 20 mgFilmtabletten Serdolect 20 mg filmuhúðaðar töflur SERDOLECT 20 mg potahované tablety Serdolect 20 mg tabletti, kalvopäällysteinen Serdolect 20 mg επικαλυμμένα με λεπτό υμένιο δισκία

apvalkotas tabletes

List of nationally authorised medicinal products EMA/580033/2017

Page 6/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 4 mg

UK/H/0141/001

BE285573

H. LUNDBECK A/S

BE

UK/H/0141/001

BE434375

H. LUNDBECK A/S

BE

UK/H/0141/001

BE184231

H. LUNDBECK A/S

BE

UK/H/0141/001

61.582

H. LUNDBECK A/S

ES

UK/H/0141/001

PL 13761/0001

H. LUNDBECK A/S

UK

UK/H/0141/001

96-0271

H. LUNDBECK A/S

NO

not available

UP/I-530-09/12-02/50

LUNDBECK CROATIA D.O.O.

HR

UK/H/0141/001

BE285573

H. LUNDBECK A/S

BE

UK/H/0141/001

BE434375

H. LUNDBECK A/S

BE

comprimés pelliculés Serdolect 4 mg comprimés pelliculés Serdolect 4 mg comprimés pelliculés Serdolect 4 mg comprimidos recubiertos con película Serdolect 4 mg filmcoated tablets Serdolect 4 mg filmdrasjerte tabletter Serdolect 4 mg filmom obložene tablete Serdolect 4 mg filmomhulde tabletten Serdolect 4 mg filmomhulde tabletten

List of nationally authorised medicinal products EMA/580033/2017

Page 7/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect 4 mg

UK/H/0141/001

RVG 20610

H. LUNDBECK A/S

NL

not available

OGYI-T-5605/01

H. LUNDBECK A/S

HU

UK/H/0141/001

1-21725

H. LUNDBECK A/S

AT

UK/H/0141/001

IS/1/02/026/01

H. LUNDBECK A/S

IS

not available

68/672/96-A/C

H. LUNDBECK A/S

CZ

UK/H/0141/001

90337/24-11-2016

LUNDBECK HELLAS, GR

GR

not available

7720/2015/01-02

H. LUNDBECK A/S

RO

UK/H/0141/001

BE184231

H. LUNDBECK A/S

BE

UK/H/0141/001

12400

H. LUNDBECK A/S

FI

filmomhulde tabletten Serdolect 4 mg filmtabletta Serdolect 4 mgFilmtabletten Serdolect 4 mg filmuhúðaðar töflur SERDOLECT 4 mg potahované tablety Serdolect 4 mg επικαλυμμένα με λεπτό υμένιο δισκία Serdolect 4 mg, comprimate filmate Serdolect 4 mg, filmomhulde tabletten Serdolect 4 mg, tabletti, kalvopäällysteinen

List of nationally authorised medicinal products EMA/580033/2017

Page 8/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect Tabletki

not available

10893

H. LUNDBECK A/S

PL

not available

10894

H. LUNDBECK A/S

PL

not available

10892

H. LUNDBECK A/S

PL

not available

168497

H. LUNDBECK A/S

EE

UK/H/0141/03

20577

H. LUNDBECK A/S

SE

not available

168597

H. LUNDBECK A/S

EE

not available

168697

H. LUNDBECK A/S

EE

not available

168397

H. LUNDBECK A/S

EE

UK/H/0141/01

20576

H. LUNDBECK A/S

SE

powlekane 12 mg Serdolect Tabletki powlekane 16 mg Serdolect Tabletki powlekane 4 mg SERDOLECT, 12 mg õhukese polümeerikattega tabletid Serdolect, 12 mg, filmdragerade tabletter SERDOLECT, 16 mg õhukese polümeerikattega tabletid SERDOLECT, 20 mg õhukese polümeerikattega tabletid SERDOLECT, 4 mg õhukese polümeerikattega tabletid Serdolect, 4 mg, filmdragerade tabletter

List of nationally authorised medicinal products EMA/580033/2017

Page 9/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Serdolect, filmovertrukne

UK/H/0141/003

18313

H. LUNDBECK A/S

DK

UK/H/0141/004

18314

H. LUNDBECK A/S

DK

UK/H/0141/005

18315

H. LUNDBECK A/S

DK

UK/H/0141/001

18311

H. LUNDBECK A/S

DK

UK/H/0141/003

38471.02.00

H. LUNDBECK A/S

DE

UK/H/0141/004

38471.03.00

H. LUNDBECK A/S

DE

UK/H/0141/005

38471.04.00

H. LUNDBECK A/S

DE

UK/H/0141/001

38471.00.00

H. LUNDBECK A/S

DE

not available

980 02 85

H. LUNDBECK A/S

BG

tabletter 12 mg Serdolect, filmovertrukne tabletter 16 mg Serdolect, filmovertrukne tabletter 20 mg Serdolect, filmovertrukne tabletter 4 mg Serdolect® 12 mg, Filmtabletten Serdolect® 16 mg, Filmtabletten Serdolect® 20 mg, Filmtabletten Serdolect® 4 mg, Filmtabletten Сердолект 12 mg филмирани таблетки

List of nationally authorised medicinal products EMA/580033/2017

Page 10/11

Product Name (in authorisation country)

MRP/DCP Authorisation number

National Authorisation Number

MAH of product in the member state

Member State where product is authorised

Сердолект 16 mg

not available

980 02 84

H. LUNDBECK A/S

BG

not available

980 02 86

H. LUNDBECK A/S

BG

филмирани таблетки Сердолект 4 mg филмирани таблетки

List of nationally authorised medicinal products EMA/580033/2017

Page 11/11

List of nationally authorised medicinal products - European Medicines ...

Sep 1, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation ... not available. 68/0516/97-S.

126KB Sizes 9 Downloads 247 Views

Recommend Documents

List of nationally authorised medicinal products - European Medicines ...
Jan 11, 2018 - LARGACTIL not available. PL 04425/0582. AVENTIS PHARMA LTD. UK. LARGACTIL 100 mg, comprimé pelliculé sécable not available. 305 712-4. SANOFI-AVENTIS FRANCE. FR. LARGACTIL 25 mg, comprimé pelliculé sécable not available. 305 711-

List of nationally authorised medicinal products - European Medicines ...
Jul 19, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation country) .... not available. 19158.

List of nationally authorised medicinal products - European Medicines ...
Sep 29, 2016 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name ... EKISTOL 50 mg comprimidos not available.

List of nationally authorised medicinal products - European Medicines ...
Jan 11, 2018 - List of nationally authorised medicinal products. EMA/24585/2018. Page 2/8. Product Name (in authorisation country). MRP/DCP Authorisation number. National Authorisation. Number. MAH of product in the member state. Member State where p

List of nationally authorised medicinal products - European Medicines ...
Jun 21, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in ... Sinemet retard-Tabletten not available.

List of nationally authorised medicinal products - European Medicines ...
Jul 6, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation country) ... not available. 68.620.

List of nationally authorised medicinal products - European Medicines ...
Sep 29, 2016 - List of nationally authorised medicinal products cilostazol. EMA/648833/2016. Page 2/3. Product Name. (in authorisation country). MRP/DCP ...

List of nationally authorised medicinal products - European Medicines ...
Mar 9, 2017 - product is authorised. AFFERA 50 microgrammes/5 microgrammes par dose, suspension pour inhalation en flacon pressurisé. UK/H/4378/001.

List of nationally authorised medicinal products - European Medicines ...
26 Oct 2017 - 30 Churchill Place ○ Canary Wharf ○ London E14 5EU ○ United Kingdom. An agency of the European Union. Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5525. Send a question via our website www.ema.europa.eu/contact. © Europ

beclometasone List of nationally authorised medicinal products ...
Sep 1, 2017 - E MA /594294/2017. P age 2 /22. Product Name (in authorisation country). MRP/DCP. Authorisation number. National Authorisation Number.

levosimendan List of nationally authorised medicinal products
Jun 9, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation ... not available. 41/0221/02-S.

chlormadinone: List of nationally authorised medicinal products ...
Sep 13, 2017 - List of nationally authorised medicinal products. Active substance: chlormadinone. Procedure no. ... Member State where product is authorised.

Quinapril: List of nationally authorised medicinal products - European ...
Dec 1, 2016 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name. (in authorisation ... not available. BE150954.

tirofiban List of nationally authorised medicinal products PSUSA-2974 ...
Jan 12, 2017 - Send a question via our website www.ema.europa.eu/contact ... Product Name (in authorisation country). MRP/DCP .... not available. 99-0206.

loperamide: List of nationally authorised medicinal products - PSUSA ...
Jan 12, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation ... not available. 00014/0611.

fenofibrate - List of nationally authorised medicinal products - PSUSA ...
Apr 12, 2018 - Member State where product is authorised. FÉNOFIBRATE BIOGARAN®. 300 mg, gélule not available. 3400936089204. BIOGARAN. FR.

List of nationally authorised medicinal products - PSUSA/00002102 ...
Jan 25, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Page 2/3. Product Name (in authorisation country) ... not available.

thiopental - List of nationally authorised medicinal products - PSUSA ...
Dec 14, 2016 - Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5525. Send a question via our ... List of nationally authorised medicinal products.

List of nationally authorised medicinal products PSUSA-00002079 ...
European Medicines Agency, 2017. Reproduction is authorised provided the source is acknowledged. 30 November 2017. EMA/812281/2017. Human Medicines Evaluation Division. List of nationally authorised medicinal products. Active substance(s): moclobemid

solifenacin: List of nationally authorised medicinal products; PSUSA ...
Feb 8, 2018 - OFFICE BE. BE. Vesicare 5 mg filmdragerad tablett. NL/H/0487/001. 19192. ASTELLAS PHARMA A/S. FI. Vesiker 5 mg, compresse rivestite con film .... 036564019. ASTELLAS PHARMA S.P.A.. IT. VESICARE 5 mg, comprimé pelliculé. NL/H/0487/001.

mefloquine - List of nationally authorised medicinal products - PSUSA ...
Oct 26, 2017 - National Authorisation Number. MAH of product in the member state. Member State where product is authorised. Lariam 250 mg Tabletten not ...

risperidone - List of nationally authorised medicinal products - PSUSA ...
με λεπτό υμένιο δισκία. Eperon 6 mg επικαλυμμένα με λεπτό υμένιο δισκία. Eperon 8 mg επικαλυμμένα με λεπτό υμένιο δισκία. Page 3. Page 4. Page 5. Page 6. Page 7. podaljÅ

rabeprazole: List of nationally authorised medicinal products - PSUSA ...
Jun 21, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation country). MRP/ .... not available.

List of nationally authorised medicinal products - PSUSA/00000294 ...
Jun 21, 2017 - Send a question via our website www.ema.europa.eu/contact. © European ... Product Name (in authorisation country). MRP/ ... not available.