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PRODUCT DETAIL

Rukobia 600 mg tablety s predĺženým uvoľňovaním

Code 0218E
MA number EU/1/20/1518/002
Product Form: tbl plg 180 (3x60)x600 mg (fľ.HDPE)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 42 - CHEMOTHERAPEUTICA (VRATANE TUBERKULOSTATIK)
ATC:
J ANTIINFECTIVES FOR SYSTEMIC USE
J05 ANTIVIRALS FOR SYSTEMIC USE
J05A DIRECT ACTING ANTIVIRALS
J05AX Other antivirals
J05AX29 Fostemsavir
Shelf life: 36
Container: bottle HDPE
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 04.02.2021
Validity: 04.02.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 04.04.2022
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