Халавен® (Halaven) инструкция по применению
- 💊 Состав препарата Халавен®
- ✅ Применение препарата Халавен®
⚠️ Регистрационное удостоверение данного продукта заменено
Дата обновления информации: 2024.09.11
Владелец регистрационного удостоверения:
ЭЙСАЙ ЮРОП, Лимитед
(Великобритания)
Вторичная упаковка:
EISAI MANUFACTURING, LTD. (Великобритания) или ФАРМСТАНДАРТ-УфаВИТА, ОАО (Россия)
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/1 мл: фл. 2 мл 1 или 6 шт.
РУ: ЛП-001782
от 24.07.12
- Заменено
Дата переоформления: 17.10.17
|
Форма выпуска, упаковка и состав препарата Халавен®
Раствор для в/в введения прозрачный, бесцветный.
| 1 мл | |
| эрибулин | 0.5 мг |
Вспомогательные вещества: этанол 0.05 мл, хлористоводородная кислота или натрия гидроксид до pH 6.0-9.0, вода д/и до 1 мл.
2 мл - флаконы бесцветного стекла (1) - пачки картонные.
2 мл - флаконы бесцветного стекла (6) - пачки картонные.
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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