France· FR:64419961
DELSTRIGO 100 mg/300 mg/245 mg, comprimé pelliculé
A medicinal product containing lamivudine + doravirine + fumarate de ténofovir disoproxil, registered in France by MERCK SHARP & DOHME (PAYS-BAS), on the national reimbursement list.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- LAMIVUDINE + DORAVIRINE + FUMARATE DE TÉNOFOVIR DISOPROXIL
- Manufacturer
- MERCK SHARP & DOHME (PAYS-BAS)
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009301613571 flacon(s) polyéthylène haute densité (PEHD) avec fermeture de sécurité enfant polypropylène de 30 comprimé(s)EUR 407.43
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lamivudine + doravirine + fumarate de ténofovir disoproxil in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaDELSTRIGOMerck Sharp & Dohme B.V., Haarlem
- FinlandDelstrigoOrifarm Oy
- United StatesDELSTRIGOMerck Sharp & Dohme LLC
- CanadaDELSTRIGOMERCK CANADA INC
- IcelandDelstrigoMerck Sharp & Dohme B.V.*
- NorwayDelstrigoMerck Sharp & Dohme Ltd (1)
- PolandDelstrigoMerck Sharp & Dohme B.V.
- SwedenDelstrigo 100 mg/300 mg/245 mg Filmdragerad tablettMerck Sharp & Dohme BV
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Delstrigo
- Liechtenstein · Delstrigo
- Norway · Delstrigo
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 Base de données publique des médicaments — BDPM (France). 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/0a85abc5-8080-4f32-8e16-823189ee8717 GET /v1/drugs/0a85abc5-8080-4f32-8e16-823189ee8717?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.
{
"cis": "64419961",
"date_amm": "2018-11-22",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/18/1333",
"substance": "LAMIVUDINE + DORAVIRINE + FUMARATE DE TÉNOFOVIR DISOPROXIL",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "comprimé pelliculé",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about lamivudine + doravirine + fumarate de ténofovir disoproxil.
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.