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PRODUCT DETAIL

Sildenafil Actavis 50 mg filmom obalené tablety

Code 9719B
MA number EU/1/09/595/017
Product Form: tbl flm 24x50 mg (blis.PVC/PVDC/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Actavis Group PTC ehf., Iceland
Therapeutic Class: 83 - VASODILATANTIA
ATC:
G GENITO URINARY SYSTEM AND SEX HORMONES
G04 UROLOGICALS
G04B UROLOGICALS (OTHER UROLOGICALS, INCL. ANTISPASMODICS-delete WHO)
G04BE Drugs used in erectile dysfunction
G04BE03 Sildenafil
Shelf life: 36
Container: blister PVDC/PVC/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 06.06.2016
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 21.06.2018
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