About the medicine
- Active ingredients
- Денозумаб + Denosumab
- INN
- ДЕНОСУМАБ
- Strength
- 120 мг
- Dosage form
- раствор для подкожного введения
- Manufacturer
- Амджен Мэньюфэкчуринг Лимитед (Пуэрто-Рико)
- Dispensing
- Prescription only
- Registration certificate
- ЛП-№001344-ГП-KZ, РК-ЛС-5№019749
- Registered
- 6 Oct 2025
- Registration valid until
- 31 Dec 2027
- Shelf life
- 3 год
- Country of registration
- Kazakhstan
Packs 1
- По 120 мг (1.7 мл) во флаконе из стекла. Флакон в пачке 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.
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).