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PRODUCT DETAIL

Renagel 800 mg filmom obalené tablety

Code 80604
MA number EU/1/99/123/013
Product Form: tbl flm 6x30x800 mg (fľa. HDPE )
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
Container: bottle HDPE
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application
MA issued: 28.01.2000
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 30.06.2021
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