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PRODUCT DETAIL

Renvela 0,8 g prášok na perorálnu suspenziu

Code 9312C
MA number EU/1/09/521/008
Product Form: plu por 90x0,8 g (vre.EAA/PET/LDPE/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Sanofi B.V., Netherland
Therapeutic Class: 87 - VARIA I
ATC:
V VARIOUS
V03 ALL OTHER THERAPEUTIC PRODUCTS
V03A ALL OTHER THERAPEUTIC PRODUCTS
V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia
V03AE02 Sevelamer
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application
MA issued: 20.09.2018
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 05.03.2019
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