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Showing 21-40 of 69 matching medicines

Product listings were last updated on 27/04/2024
Trade Name Licence Number & Holder Documents
Ramonna 1500 microgram Tablet
Tablet

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PA1330/021/001
Authorised: 03/02/2006
Gedeon Richter Plc
SPC PIL
Ranexa
Prolonged-release tablet

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EU/1/08/462/1,2,7,8
Authorised: 09/07/2008
Menarini International Operations Luxembourg S.A.
SPC PIL IPAR
Ranexa 500 mg prolonged-release tablets
Prolonged-release tablet

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EU/1/08/462/3,4,9,10

Menarini International Operations Luxembourg S.A.
SPC PIL IPAR
Ranexa 750 mg prolonged-release tablets
Prolonged-release tablet

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EU/1/08/462/5,6,11,12

Menarini International Operations Luxembourg S.A.
SPC PIL IPAR
Raniviso
Solution for injection

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EU/1/22/1673/001
Authorised: 25/08/2022
Midas Pharma GmbH
SPC PIL IPAR EdM
Ranolazine 375 mg Prolonged-release tablet
Prolonged-release tablet

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PA23245/003/001
Authorised: 29/07/2022
Elc Group s.r.o.
SPC PIL
Ranolazine 500 mg Prolonged-release tablet
Prolonged-release tablet

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PA23245/003/002
Authorised: 29/07/2022
Elc Group s.r.o.
SPC PIL
Ranolazine 750 mg Prolonged-release tablet
Prolonged-release tablet

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PA23245/003/003
Authorised: 29/07/2022
Elc Group s.r.o.
SPC PIL
Ranolazine Clonmel 375 mg prolonged-release tablets
Prolonged-release tablet

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PA0126/356/001
Authorised: 29/07/2022
Clonmel Healthcare Ltd
SPC PIL
Ranolazine Clonmel 500 mg prolonged-release tablets
Prolonged-release tablet

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PA0126/356/002
Authorised: 29/07/2022
Clonmel Healthcare Ltd
SPC PIL
Ranolazine Clonmel 750 mg prolonged-release tablets
Prolonged-release tablet

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PA0126/356/003
Authorised: 29/07/2022
Clonmel Healthcare Ltd
SPC PIL
Ranolazine Krka 375 mg prolonged release tablets
Prolonged-release tablet

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PA1347/109/001
Authorised: 31/03/2023
KRKA, d.d., Novo mesto
SPC PIL
Ranolazine Krka 500 mg prolonged release tablets
Prolonged-release tablet

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PA1347/109/002
Authorised: 31/03/2023
KRKA, d.d., Novo mesto
SPC PIL
Ranolazine Krka 750 mg prolonged release tablets
Prolonged-release tablet

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PA1347/109/003
Authorised: 31/03/2023
KRKA, d.d., Novo mesto
SPC PIL
Rapamune
Oral solution

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EU/1/01/171/001
Authorised: 13/03/2001
Pfizer Europe MA EEIG
SPC PIL IPAR
Rapamune
Oral solution

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EU/1/01/171/002
Authorised: 13/03/2001
Pfizer Europe MA EEIG
SPC PIL IPAR
Rapamune
Oral solution

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EU/1/01/171/005
Authorised: 13/03/2001
Pfizer Europe MA EEIG
SPC PIL IPAR
Rapamune
Coated tablet

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EU/1/01/171/007
Authorised: 12/04/2002
Pfizer Europe MA EEIG
SPC PIL IPAR
Rapamune
Coated tablet

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EU/1/01/171/008
Authorised: 12/04/2002
Pfizer Europe MA EEIG
SPC PIL IPAR
Rapamune
Coated tablet

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EU/1/01/171/009-010
Authorised: 10/01/2003
Pfizer Europe MA EEIG
SPC PIL IPAR