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PRODUCT DETAIL

Onureg 300 mg filmom obalené tablety

Code 8017D
MA number EU/1/21/1556/003
Product Form: tbl flm 7x300 mg (blis.OPA/PVC/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01B ANTIMETABOLITES
L01BC Pyrimidine analogues
L01BC07 Azacitidine
Shelf life: 36
Container: blister OPA/Al/PVC
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - known active substance
MA issued: 17.06.2021
Validity: 17.06.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 30.06.2021
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