Халавен® (Halaven) инструкция по применению
- 💊 Состав препарата Халавен®
- ✅ Применение препарата Халавен®
⚠️ Государственная регистрация данного препарата отменена
Дата обновления информации: 2024.05.22
Владелец регистрационного удостоверения:
ЭЙСАЙ ЮРОП, Лимитед
(Великобритания)
Упаковка и выпускающий контроль качества:
EISAI MANUFACTURING, LTD. (Великобритания) или ФАРМСТАНДАРТ-УфаВИТА, ОАО (Россия)
Код ATX:
L01XX41
(Эрибулин)
Лекарственная форма
Препарат отпускается по рецепту
|
Халавен® |
Раствор для внутривенного введения 0.5 мг/мл: фл. 2 мл 1 или 6 шт.
РУ: ЛП-№(003562)-(РГ-RU)
от 31.10.23
- Отмена гос. регистрации
Предыдущий РУ: ЛП-001782
|
Форма выпуска, упаковка и состав препарата Халавен®
Раствор для в/в введения прозрачный бесцветный.
| 1 мл | 1 фл. | |
| эрибулина мезилат | 0.5 мг | 1 мг |
Вспомогательные вещества: этанол, хлористоводородная кислота (для коррекции pH), натрия гидроксид (для коррекции pH), вода д/и.
2 мл - флаконы из прозрачного бесцветного гидролитического стекла типа I номинальной вместимостью 5 мл (1) - пачки картонные.
2 мл - флаконы из прозрачного бесцветного гидролитического стекла типа I номинальной вместимостью 5 мл (6) - пачки картонные.
Места вскрытия пачки заклеены двумя прозрачными защитными стикерами.
Клинико-фармакологическая группа:
Противоопухолевый препарат
Фармако-терапевтическая группа:
Противоопухолевое средство
Адрес производителя
| БСП Фармасьютикалс , С.п.А. | Италия | Via Appia Km 65, 561 (loc. Latina Scalo) - 04013 Latina (LT), Italy |
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