Source: European Medicines Agency (EU) Revision Year: 2023 Publisher: bbVie Deutschland GmbH & Co. KG, Knollstrasse, 67061 Ludwigshafen, Germany
Maviret 100 mg/40 mg film-coated tablets.
Pharmaceutical Form |
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Film-coated tablet (tablet). Pink, oblong, biconvex, film-coated tablet of dimensions 18.8 mm x 10.0 mm, debossed on one side with ‘NXT’. |
Each film-coated tablet contains 100 mg glecaprevir and 40 mg pibrentasvir.
Excipient with known effect: Each film-coated tablet contains 7.48 mg lactose (as lactose monohydrate).
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Glecaprevir |
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Glecaprevir and Pibrentasvir |
Glecaprevir/Pibrentasvir is a fixed-dose combination of two pan-genotypic, direct-acting antiviral agents, glecaprevir (NS3/4A protease inhibitor) and pibrentasvir (NS5A inhibitor), targeting multiple steps in the HCV viral lifecycle. |
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Pibrentasvir |
Pibrentasvir is a pan-genotypic inhibitor of HCV nonstructural protein 5A (NS5A), which is essential for viral RNA replication and virion assembly. |
List of Excipients |
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Tablet core: Copovidone (Type K 28) Film coating: Hypromellose 2910 (E464) |
PVC/PE/PCTFE aluminium foil blister packs.
Pack containing 84 (4 cartons of 21 tablets) film-coated tablets.
bbVie Deutschland GmbH & Co. KG, Knollstrasse, 67061 Ludwigshafen, Germany
EU/1/17/1213/001
Date of first authorisation: 26 July 2017
Date of latest renewal: 22 March 2022
Drug | Countries | |
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MAVIRET | Austria, Australia, Brazil, Canada, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom |
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