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PRODUCT DETAIL

Abiraterón Krka 500 mg filmom obalené tablety

Code 8020D
MA number EU/1/21/1553/001
Product Form: tbl flm 56x500 mg (blis.PVC/PE/PVDC//papier/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L02 ENDOCRINE THERAPY
L02B HORMONE ANTAGONISTS AND RELATED AGENTS
L02BX Other hormone antagonists and relate agents
L02BX03 Abiraterone
Shelf life: 24
Container: blister PVC/PE/PVDC/Al/paper
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 24.06.2021
Validity: 24.06.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 01.07.2021
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