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PRODUCT DETAIL

Aclasta 5 mg infúzny roztok

Code 90197
MA number EU/1/05/308/001
Product Form: sol inf 1x100 ml/5 mg (fľ.plast.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 87 - VARIA I
ATC:
M MUSCULO-SKELETAL SYSTEM
M05 DRUGS FOR TREATMENT OF BONE DISEASES
M05B DRUGS AFFECTING BONE STRUCTURE AND MINERALIZATION
M05BA Bisphosphonates
M05BA08 Zoledronic acid
Shelf life: 36
Container: bottle plastic
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - known active substance
MA issued: 15.04.2005
SmPC + PL: European Medicines Agency's database
Dokument: Aclasta_DHCP_SK.pdf  
Safety feature Yes
Data update: 14.06.2018
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