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EMA approval · 2026-02-06

EMA Authorised: Rayvow (lasmiditan succinate) — Eli Lilly Nederland B.V.

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Summary

The EMA authorised Rayvow (lasmiditan succinate) for migraine disorders; the product is manufactured by Eli Lilly Nederland B.V.

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Diseases / indications

Drugs mentioned

  • Rayvow (lasmiditan succinate)

Snippet

Status: Authorised. Therapeutic area: Migraine Disorders. MAH: Eli Lilly Nederland B.V.. Decision date: 05/02/2026