Catalyst Wire Dossier Catalyst Wire Dossier
EMA approval · 2022-06-09

EMA Authorised: Desloratadine Teva (desloratadine) — Teva B.V

View source ↗

Summary

The EMA authorised Desloratadine Teva (desloratadine) for allergic rhinitis (perennial and seasonal) with Teva B.V. as the marketing authorization holder.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • Desloratadine Teva (desloratadine)

Snippet

Status: Authorised. Therapeutic area: Rhinitis, Allergic, Perennial;Rhinitis, Allergic, Seasonal. MAH: Teva B.V. Decision date: 30/05/2022