Levetiracetam Actavis

Страна: Новая Зеландия

Язык: английский

Источник: Medsafe (Medicines Safety Authority)

Купи это сейчас

Активный ингредиент:

Levetiracetam 500mg;  

Доступна с:

Teva Pharma (New Zealand) Limited

ИНН (Международная Имя):

Levetiracetam 500 mg

дозировка:

500 mg

Фармацевтическая форма:

Film coated tablet

состав:

Active: Levetiracetam 500mg   Excipient: Colloidal silicon dioxide Crospovidone Magnesium stearate Opadry yellow 85F32371 Povidone

Тип рецепта:

Prescription

Производитель:

Neuland Laboratories Limited

Терапевтические показания :

Use in epileptic patients aged 4 years and older, initially as add on therapy, in the treatment of partial onset seizures with or without secondary generalisation. Monotherapy in the treatment of partial onset seizures, with or without secondary generalisation, in patients from 16 years of age with newly diagnosed epilepsy. Add on therapy in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with Juvenile Myoclonic Epilepsy (JME). Add on therapy in the treatment of primary generalized tonic-clonic seizures in adults and children from 4 years of age with idiopathic generalized epilepsy (IGE).

Обзор продуктов:

Package - Contents - Shelf Life: Blister pack, PVC/Al - 60 tablets - 36 months from date of manufacture stored at or below 25°C - Bottle, plastic, HDPE with LDPE screw cap and tamper evident - 100 tablets - 36 months from date of manufacture stored at or below 25°C

Дата Авторизация:

2015-01-22

Поиск оповещений, связанных с этим продуктом

Просмотр истории документов