Кувитру
Раствор для подкожного введения
Prescription only
About the medicine
- Strength
- 1 г, 2 г, 4 г, 8 г
- Dosage form
- Раствор для подкожного введения
- Manufacturer
- Баксалта Бельгия Мануфактуринг С.А. (Бельгия)
- Dispensing
- Prescription only
- Registration certificate
- РК-ЛС-5№024863
- Registered
- 29 Dec 2020
- Registration valid until
- 5 Nov 2027
- Shelf life
- 2 год
- Country of registration
- Kazakhstan
Packs 1
- По 5, 10, 20 и 40 мл препарата во флаконе. По одному флакону в коробке из картона.
Package leaflet
There is no leaflet with these active ingredients in the reference yet. Read the leaflet in the pack and ask a doctor or pharmacist.
Other forms and manufacturers
This is reference information and does not replace a doctor's advice. Do not self-medicate: read the leaflet and ask a specialist before use.
Source: State Register of Medicines of the Republic of Kazakhstan (register.ndda.kz).