Europe 25 mg/ml, koncentrat do sporządzania roztworu do infuzji Normosang 25 mg/ml – infuusiokonsentraatti liuosta varten Normosang 25 mg/ml Konzentrat zur Herstellung einer Infusionslösung Normosang 25 mg/ml Konzentrat zur Herstellung einer Infusionslösung Normosang 25 mg/ml infusioonilahuse kontsentraat NORMOSANG 25 mg/ml infúzny koncentrát Normosang 25 mg/ml innrennslisþykkni, lausn Normosang 25 mg/ml koncentrat za otopinu za infuziju
List of nationally authorised medicinal products EMA/28573/2017
Page 2/5
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
Normosang 25 mg/ml
FR/H/140/01
H/09/01129/001
ORPHAN EUROPE SARL
SI
FR/H/0140/001
LT/1/08/1024/001
ORPHAN EUROPE SARL
LT
FR/H/0140/001
06-0218
ORPHAN EUROPE SARL
LV
FR/H/0140/001
OGYI-T-20408/01
ORPHAN EUROPE SARL
HU
FR/H/0140/001
BE207496
ORPHAN EUROPE SARL
BE
FR/H/0140/001
RVG 33614
ORPHAN EUROPE SARL
NL
FR/H/0140/001
2938082
ORPHAN EUROPE SARL
PT
FR/H/0140/001
63.116
ORPHAN EUROPE SARL
ES
FR/H/140/01
PA928/1/1
ORPHAN EUROPE SARL
IE
koncentrat za raztopino za infundiranje Normosang 25 mg/ml koncentratas infuziniam tirpalui NORMOSANG 25 mg/ml koncentrāts infūziju šķīduma pagatavošanai Normosang 25 mg/ml koncentrátum oldatos infúzióhoz Normosang 25 mg/ml, concentraat voor oplossing voor infusie Normosang 25 mg/ml, concentraat voor oplossing voor infusie Normosang 25 mg/ml, concentrado para solução para perfusão NORMOSANG 25 mg/ml, concentrado para solution para perfusion NORMOSANG 25 mg/ml, concentrate for solution for infusion
List of nationally authorised medicinal products EMA/28573/2017
Page 3/5
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
NORMOSANG 25 mg/ml,
FR/H/140/01
PL 15266/0008
ORPHAN EUROPE SARL
UK
FR/H/0140/001
034543013/M
ORPHAN EUROPE SARL
IT
FR/H/0140/001
MA135/00101
ORPHAN EUROPE SARL
MT
FR/H/0140/001
80/271/06-C
ORPHAN EUROPE SARL
CZ
FR/H/0140/001
15349
ORPHAN EUROPE SARL
SE
FR/H/140/01
06-3943
ORPHAN EUROPE SARL
NO
FR/H/0140/001
BE207496
ORPHAN EUROPE SARL
BE
FR/H/0140/001
0084/99/07/0010
ORPHAN EUROPE SARL
LU
concentrate for solution for infusion Normosang 25 mg/mL, concentrato per soluzione per infusione Normosang 25 mg/ml, konċentrat għal soluzzjoni għall-infużjoni. Normosang 25 mg/ml, koncentrát pro infuzní roztok Normosang 25 mg/ml, koncentrat till infusionsvätska, lösning Normosang 25 mg/ml, konsentrat til infusjonsvæske Normosang 25 mg/ml, Konzentrat zur Herstellung einer Infusionslösung Normosang 25 mg/ml, Konzentrat zur Herstellung einer Infusionslösung
List of nationally authorised medicinal products EMA/28573/2017
Page 4/5
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
Normosang 25 mg/ml,
FR/H/0140/001
BE207496
ORPHAN EUROPE SARL
BE
FR/H/0140/001
34009 558 611 1 9
ORPHAN EUROPE SARL
FR
FR/H/140/01
26M0019
ORPHAN EUROPE SARL
CY
FR/H/0140/001
18966/22-10-99
ORPHAN EUROPE SARL
GR
FR/H/0140/001
30617
ORPHAN EUROPE SARL
DK
solution à diluer pour perfusion Normosang 25 mg/ml, solution à diluer pour perfusion Normosang 25 mg/ml, πυκνό διάλυμα για παρασκευή διαλύματος προς έγχυση. Normosang 25 mg/ml, πυκνό διάλυμα για παρασκευή διαλύματος προς έγχυση Normosang, koncentrat til infusionsvæske, opløsning
List of nationally authorised medicinal products EMA/28573/2017
Sep 13, 2017 - List of nationally authorised medicinal products. Active substance: chlormadinone. Procedure no. ... Member State where product is authorised.
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
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.
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
Oct 26, 2017 - National Authorisation Number. MAH of product in the member state. Member State where product is authorised. Lariam 250 mg Tabletten not ...
