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Showing 21-35 of 35 matching medicines

Product listings were last updated on 28/06/2022
Trade Name Licence Number & Holder Documents
Xenleta
Film-coated tablet

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EU/1/20/1457/002
Authorised: 27/07/2020
Nabriva Therapeutics Ireland DAC
SPC PIL IPAR Variations
Xenleta
Concentrate and solvent for solution for infusion

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EU/1/20/1457/001
Authorised: 27/07/2020
Nabriva Therapeutics Ireland DAC
SPC PIL IPAR Variations
XEOMIN 100 units powder for solution for injection
Powder for solution for injection

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PA1907/001/002
Authorised: 31/01/2014
Merz Pharmaceuticals GmbH
SPC PIL
XEOMIN 200 units powder for solution for injection
Powder for solution for injection

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PA1907/001/003
Authorised: 01/07/2016
Merz Pharmaceuticals GmbH
SPC PIL
XEOMIN 50 units powder for solution for injection
Powder for solution for injection

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PA1907/001/001
Authorised: 31/01/2014
Merz Pharmaceuticals GmbH
SPC PIL
Xeplion
Prolonged-release solution for injection

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EU/1/11/672/001
Authorised: 04/03/2011
Janssen-Cilag International NV
SPC PIL IPAR Variations
Xeplion
Prolonged-release solution for injection

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EU/1/11/672/002
Authorised: 04/03/2011
Janssen-Cilag International NV
SPC PIL IPAR Variations
Xeplion
Prolonged-release solution for injection

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EU/1/11/672/003
Authorised: 04/03/2011
Janssen-Cilag International NV
SPC PIL IPAR Variations
Xeplion
Prolonged-release solution for injection

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EU/1/11/672/004
Authorised: 04/03/2011
Janssen-Cilag International NV
SPC PIL IPAR Variations
Xeplion
Prolonged-release solution for injection

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EU/1/11/672/005-006
Authorised: 04/03/2011
Janssen-Cilag International NV
SPC PIL IPAR Variations
Xerava
Powder for concentrate for solution for infusion

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EU/1/18/1312/001
Authorised: 20/09/2018
PAION Deutschland GmbH
SPC PIL IPAR Variations
Xerava
Powder for concentrate for solution for infusion

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EU/1/18/1312/003-004
Authorised: 20/09/2018
Tetraphase Pharmaceuticals Ireland Limited
SPC PIL IPAR Variations
Xermelo
Film-coated tablet

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EU/1/17/1224/001-002
Authorised: 18/09/2017
Ipsen Pharma
SPC PIL IPAR Variations
Xevudy
Concentrate for solution for infusion

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EU/1/21/1562/001
Authorised: 17/12/2021
GlaxoSmithKline (Ireland) Limited
SPC PIL IPAR Variations
XGEVA
Solution for injection

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EU/1/11/703/001-002

Amgen Europe B.V.
SPC PIL IPAR EdM Variations