Source: European Medicines Agency (EU) Revision Year: 2018 Publisher: sanofi-aventis groupe, 54, rue La Boรฉtie, F-75008, Paris, France
MULTAQ 400 mg film-coated tablets.
Pharmaceutical Form |
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Film-coated tablet (tablet). White, oblong shaped tablets, engraved with a double wave marking on one side and "4142"code on the other side. |
Each tablet contains 400 mg of dronedarone (as hydrochloride).
Excipient with known effect: Each tablet also contains 41.65 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Dronedarone |
Dronedarone is a multichannel blocker inhibiting the potassium currents (including IK(Ach), IKur, IKr, IKs) and thus prolonging cardiac action potential and refractory periods (Class III). It also inhibits the sodium currents (Class Ib) and the calcium currents (Class IV). It non-competitively antagonises adrenergic activities (Class II). |
List of Excipients |
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Tablet core: Hypromellose (E464) Tablet coat: Hypromellose (E464) |
Not all pack sizes may be marketed.
sanofi-aventis groupe, 54, rue La Boรฉtie, F-75008, Paris, France
EU/1/09/591/001 – Cartons of 20 film-coated tablets
EU/1/09/591/002 – Cartons of 50 film-coated tablets
EU/1/09/591/003 – Cartons of 60 film-coated tablets
EU/1/09/591/004 – Cartons of 100 × 1 film-coated tablets
Date of first authorisation: 26 November 2009
Date of latest renewal: 22 September 2014
Drug | Countries | |
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MULTAQ | Austria, Canada, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Italy, Lithuania, Poland, Singapore, United Kingdom, United States |
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