Из оборота отозваны оставшиеся упаковки препарата «Глюкозамин Эвалар»
Компания «ЭВАЛАР» информирует об отзыве из обращения лекарственного средства «ГЛЮКОЗАМИН ЭВАЛАР», упаковки которого остались на рынке после отмены государственной регистрации. Информационное письмо об этом опубликовано 30 ноября на сайте Росздравнадзора.
Речь идёт о сериях 0048791219, 0058791219, 0018791220, 0028791220, 0038791220, 0018790421, 0028790421 и 0038790421 лекарственного препарата «ГЛЮКОЗАМИН ЭВАЛАР, порошок для приготовления раствора для приёма внутрь, 1500 мг, пакетики (20), пачки картонные» производства ЗАО «ЭВАЛАР» (Россия).
Государственная регистрация этого ЛС была отменена по решению владельца регистрационного удостоверения в начале ноября.
Напоминаем, что реализация ЛС после отмены их государственной регистрации является административным нарушением и расценивается как «Продажа или ввоз на территорию Российской Федерации недоброкачественных лекарственных средств, либо реализация или ввоз недоброкачественных медицинских изделий, либо незаконные производство, продажа или ввоз незарегистрированных лекарственных средств» (ч. 2 статьи 6.33 КоАП РФ). Наказанием за это нарушение может служить крупный штраф в несколько сотен тысяч рублей.
Ранее из оборота были отозваны препараты «Гепатромбин» и «Гепатробмин С» в связи с отменой государственной регистрации этих торговых наименований.
«Катрен-Стиль» регулярно публикует обзоры информационных писем Росздравнадзора, посвящённых отзыву и изъятию ЛС, а также списки препаратов, лишившихся регистрации в течение месяца. Большое количество данных в таких статьях организовано в виде таблиц — по ним удобно проверять свой ассортимент на наличие таких ЛС. Последний обзор с перечнем таких ЛС читайте по этой ссылке.
1 декабря 2022
Фото: © Kzenon / Фотобанк Фотодженика
Выпуск: №228, декабрь 2022918 просмотров
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