EMA Recommends EU-Wide Desloratadine Switch

Teva subsidiary Ratiopharm has secured EMA's backing for the EU-wide switch of allergy drug desloratadine, representing the second reclassification approved by the regulator this year.

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Consumers across the EU are set to benefit from a new OTC option to relieve allergy symptoms after the European Medicines Agency gave the green light to the centralised switch of Ratiopharm GmbH’s Desloratadine Ratiopharm.

Desloratadine Ratiopharm – which was approved for Rx use throughout the EU in 2012 as a generic equivalent to Merck & Co. Inc.’s Aerius – is poised to become the sixth drug to be switched through EMA’s centralised procedure, making it available without a prescription in all 27 EU member states, plus in the European Economic Area countries Iceland, Liechtenstein and Norway

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