France· FR:61294762
EMTRIVA 200 mg, gélule
A emtricitabine product containing emtricitabine, registered in France by GILEAD SCIENCES IRELAND UC (IRLANDE), on the national reimbursement list. The same ATC class is registered in 13 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
Where it is registered
Emtricitabine is registered in 13 of 19 countries.
Countries holding a registration under ATC J05AF09 (emtricitabine), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 9 of them publish a price we can compare per daily dose
Emtricitabine · ATC J05AF09
13 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of emtricitabine costs, country by country.
Normalised to the WHO defined daily dose (0.2 g), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Emtricitabine · price per daily dose (0.2 g)
USD · FX 28 Sept 2026
- CH Switzerland$8.60
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- EMTRICITABINE
- Manufacturer
- GILEAD SCIENCES IRELAND UC (IRLANDE)
- Country
- France (FR)
- ATC code
- J05AF09
- ATC class
- Emtricitabine
- Defined daily dose
- 0.2 g, O
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip133400936225640flacon(s) polyéthylène haute densité (PEHD) de 30 gélules avec fermeture de sécurité enfantEUR 153.06
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
32 interactions on record for emtricitabine.
Graded by severity as the source publishes them — 4 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
Emtricitabine · interactions on record
32 records
- 4 severe
- 23 moderate
- 1 minor
Most severe, free to view
- LeflunomidL04AA13severe
- TeriflunomidL04AA31severe
- LeflunomideL04AK01severe
- TeriflunomideL04AK02severe
4 more interactions with mechanism and management, from a commercially licensed source.
Sign in to check- 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
Emtricitabine in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesemtricitabineCipla USA Inc.
- FinlandEmtrivaGilead Sciences Ireland UC
- CzechiaEMTRIVAGilead Sciences Ireland UC, Carrigtohill
- United KingdomEmtriva 200mg capsulesGilead Sciences Ltd
- BelgiumEmtriva 200 mgGilead Sciences Ireland UC
- IcelandEmtrivaGilead Sciences Ireland UC*
- NetherlandsEmtriva 200 mg, harde capsulesGilead Sciences Ireland UC
- NorwayEmtrivaGilead Sciences Ireland UC
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Spain · Emtricitabina/Tenofovir Alafenamida Dr. Reddys
- Iceland · Emtriva
- Liechtenstein · Emtriva
- Norway · Emtriva
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/7537a0f7-54dd-4ab9-b289-a1ab5f7e8f73 GET /v1/drugs/7537a0f7-54dd-4ab9-b289-a1ab5f7e8f73?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": "61294762",
"date_amm": "2003-10-24",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/03/261",
"substance": "EMTRICITABINE",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "gélule",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about emtricitabine.
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.