Netherlands· NL-042ed9c4d570
Rayvow 50 mg filmomhulde tabletten
A lasmiditan product containing lasmiditanhemisuccinaat, registered in Netherlands by Eli Lilly Nederland B.V.. The same ATC class is registered in 9 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Lasmiditan is registered in 9 of 19 countries.
Countries holding a registration under ATC N02CC08 (lasmiditan), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 6 of them publish a price we can compare per daily dose
Lasmiditan · ATC N02CC08
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- LASMIDITANHEMISUCCINAAT
- Manufacturer
- Eli Lilly Nederland B.V.
- Country
- Netherlands (NL)
- ATC code
- N02CC08
- ATC class
- Lasmiditan
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/21/1587
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
191 interactions on record for lasmiditan.
Graded by severity as the source publishes them — 19 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Lasmiditan · interactions on record
191 records
- 19 severe
- 172 moderate
Most severe, free to view
- OndansetronA04AA01severe
- GranisetronA04AA02severe
- DolasetronA04AA04severe
- PalonosetronA04AA05severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Lasmiditan in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaRAYVOWEli Lilly Nederland B.V., Utrecht
- SpainRAYVOW 50 MG COMPRIMIDOS RECUBIERTOS CON PELICULAEli Lilly Nederland B.V.
- FinlandRAYVOWEli Lilly Nederland B.V.
- IrelandRAYVOW 50 mg film-coated tabletsEli Lilly Nederland B.V.
- IcelandRayvowEli Lilly Nederland B.V.*
- PolandRayvowEli Lilly Nederland B.V.
- BelgiumRayvow 50 mgEli Lilly Nederland
- SwedenRAYVOW 50 mg Filmdragerad tablettEli Lilly Nederland B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Rayvow
- Liechtenstein · Rayvow
- Norway · Rayvow
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of CBG-MEB (Netherlands). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/7ba6535e-45b6-405f-a271-d8174c7c0729 GET /v1/drugs/7ba6535e-45b6-405f-a271-d8174c7c0729?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"form": "Filmomhulde tablet",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/rayvow-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Lasmiditan",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp127596",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"IJZEROXIDE ZWART (E 172)",
"MACROGOL 3350",
"MAGNESIUMSTEARAAT (E 470b)",
"NATRIUMLAURILSULFAAT",
"POLYVINYLALCOHOL (E 1203)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)",
"ZETMEEL, GEPREGELATINEERD"
],
"substances": [
"LASMIDITANHEMISUCCINAAT"
],
"leaflet_url": null,
"authorised_at": "2022/08/17",
"procedure_number": "EMEA/H/C/005332",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/21/1587",
"additional_monitoring": "N"
}See everything about lasmiditan.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.