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PRODUCT DETAIL

Zeffix 100 mg filmom obalené tablety

Code 02085
MA number EU/1/99/114/001
Product Form: tbl flm 28x100 mg (blis.Al/PVC)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: GlaxoSmithKline (Ireland) Limited, Ireland
Therapeutic Class: 42 - CHEMOTHERAPEUTICA (VRATANE TUBERKULOSTATIK)
ATC:
J ANTIINFECTIVES FOR SYSTEMIC USE
J05 ANTIVIRALS FOR SYSTEMIC USE
J05A DIRECT ACTING ANTIVIRALS
J05AF Nucleoside and nucleotide reverse transcriptase inhibitors
J05AF05 Lamivudine
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 29.07.1999
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 03.08.2023
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