List of nationally authorised medicinal products EMA/173192/2017
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Product Name (in authorisation country)
MRP/DCP Authorisation number not available
National Authorisation Number
MAH of product in the member state
Member State where product is authorised
2905982
PT
Mephaquin Lactab, 250 mg, comprimido revestido
not available
4506481
Mephaquin Lactab, 250 mg, comprimido revestido
not available
2906089
Lariam 250 mg tabletter
not available
10721
MEPHA-INVESTIGACAO DESENVOLVIMENTO E FABRICACAO FARMACEUTICA, LDA. MEPHA-INVESTIGACAO DESENVOLVIMENTO E FABRICACAO FARMACEUTICA, LDA. MEPHA-INVESTIGACAO DESENVOLVIMENTO E FABRICACAO FARMACEUTICA, LDA. ROCHE AB
Lariam 250 mg tabletter
not available
10721
ROCHE AB
SE
Lariam 250 mg tablets
not available
PL 00031/0236
ROCHE PRODUCTS LTD
UK
Lariam 250 mg tablets
not available
PL 00031/0236
ROCHE PRODUCTS LTD
UK
Mephaquin Lactab, 250 mg, comprimido revestido
List of nationally authorised medicinal products EMA/173192/2017
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 ...
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
Jun 21, 2017 - Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5525 ... List of nationally authorised medicinal products ... MAH of product in the.
Mar 8, 2018 - MAH of product in the member state. Member State where product is authorised. Rapibloc, pulver til infusionsvæske, opløsning. NL/H/3368/001.
Dec 13, 2017 - number. National Authorisation Number. MAH of product in the member state. Member State where product is authorised. ФоÑÑенол 750 mg.
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