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Showing 101-120 of 949 matching medicines

Product listings were last updated on 18/10/2019
Trade Name Licence Number & Holder Documents
Actonel 5 mg film coated tablets
5 milligram(s) Film-coated tablet


Generics List: Risedronic Acid (Risedronate) 5mg Film-coated Tablets

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PA2315/140/001
Authorised: 06/07/2018
Accord Healthcare Ireland Ltd.
SPC PIL
Actonel 75 mg Film Coated Tablets
75 milligram(s) Film-coated tablet


Generics List: Risedronic Acid (Risedronate) 75mg Film-coated Tablets

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PA2315/140/004
Authorised: 06/07/2018
Accord Healthcare Ireland Ltd.
SPC
Actonel Combi 35mg + 500mg film-coated tablets
35/500 milligram(s) Film-coated tablet

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PA22668/001/001
Authorised: 18/03/2005
Theramex Ireland Limited
SPC
Actonel Once A Week 35 mg film-coated tablets
35 milligram(s) Film-coated tablet


Generics List: Risedronic Acid (Risedronate) 35mg Film-coated Tablets

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PA2315/140/003
Authorised: 06/07/2018
Accord Healthcare Ireland Ltd.
SPC PIL
Actonel Once a Week 35 mg film-coated tablets
35 milligram(s) Film-coated tablet

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PPA1463/023/001
Authorised: 03/07/2009
IMED Healthcare Ltd.
SPC PIL
Actonel Once a Week 35 mg gastro-resistant tablets
35 milligram(s) Gastro-resistant tablet

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PA2315/140/005
Authorised: 06/07/2018
Accord Healthcare Ireland Ltd.
SPC PIL
Actonel Once a week 35mg Film-coated tablets
35 milligram(s) Film-coated tablet


Generics List: Risedronic Acid (Risedronate) 35mg Film-coated Tablets

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PPA0465/165/001
Authorised: 04/11/2005
PCO Manufacturing
SPC PIL
Actonel Plus Ca & D 35mg film-coated tablets + 1000mg/880 IU Effervescent Granules
35 mg + 1000 mg/800 international unit(s) Effervescent granules

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PPA0465/305/001
Authorised: 08/03/2013
PCO Manufacturing Ltd.
SPC PIL
Actonel Plus Ca & D 35mg film-coated tablets + 1000mg/880 IU Effervescent Granules
35 + 1000/880 IU milligram(s) Effervescent granules

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PA22668/002/001
Authorised: 12/10/2007
Theramex Ireland Limited
SPC
Actos
15 milligram(s) Tablet

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EU/1/00/150/001
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
15 milligram(s) Tablet

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EU/1/00/150/002
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
15 milligram(s) Tablet

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EU/1/00/150/003
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
30 milligram(s) Tablet

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EU/1/00/150/004
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
30 milligram(s) Tablet

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EU/1/00/150/005
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
30 milligram(s) Tablet

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EU/1/00/150/006
Authorised: 13/10/2000
Takeda Pharma A/S
SPC PIL IPAR EdM
Actos
45 milligram(s) Tablet

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EU/1/00/150/011
Authorised: 16/09/2003
Takeda Pharma A/S
SPC PIL IPAR EdM
Actraphane
percent volume/volume Solution for injection

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EU/1/02/229/001-035
Authorised: 07/10/2002
Novo Nordisk A/S
SPC PIL IPAR
ACTRAPHANE 30
40 IU/ML Suspension for Injection

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EU/1/02/229/036-037
Authorised: 13/08/2003
Novo Nordisk A/S
SPC PIL IPAR
Actrapid
international unit(s)/millilitre Solution for injection

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EU/1/02/230/001-015
Authorised: 07/10/2002
Novo Nordisk A/S
SPC PIL IPAR
ACTRAPID
40/100 IU/ML Solution for Injection

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EU/1/02/230/016-017
Authorised: 13/08/2003
Novo Nordisk A/S
SPC PIL IPAR