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PRODUCT DETAIL

REKAMBYS 900 mg injekčná suspenzia s predĺženým uvoľňovaním

Code 6276D
MA number EU/1/20/1482/002
Product Form: sus ijp 1x3 ml/900 mg (liek.inj.skl.)
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
J05AG Non-nucleoside reverse transcriptase inhibitors
J05AG05 Rilpivirine
Shelf life: 36
Container: glass vial
Route of admin.: Intramuscular use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - known active substance
MA issued: 21.12.2020
Validity: 21.12.2025
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 07.03.2023
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