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PRODUCT DETAIL

Desloratadine Actavis 5 mg filmom obalené tablety

Code 0365B
MA number EU/1/11/745/010
Product Form: tbl flm 30x5 mg (fľ.HDPE)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Actavis Group PTC ehf., Iceland
Therapeutic Class: 24 - ANTIHISTAMINICA, HISTAMIN
ATC:
R RESPIRATORY SYSTEM
R06 ANTIHISTAMINES FOR SYSTEMIC USE
R06A ANTIHISTAMINES FOR SYSTEMIC USE
R06AX Other antihistamines for systemic use
R06AX27 Desloratadine
Shelf life: 36
Container: blister OPA/Al/PVC/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 13.01.2012
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 08.01.2020
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