Switzerland· 63165002
Zyclara, Crème
A imiquimod product containing imiquimodum, registered in Switzerland by Viatris Pharma GmbH and dispensed under Swissmedic category A, on the national reimbursement list. The same ATC class is registered in 16 of our 19 countries.
Checked against Swissmedic (Switzerland) on
Informational only — not a medical device.
Where it is registered
Imiquimod is registered in 16 of 19 countries.
Countries holding a registration under ATC D06BB10 (imiquimod), each read from that country’s own register.
- This record: Switzerland, from Swissmedic (Switzerland)
- 10 of them publish a price we can compare per daily dose
Imiquimod · ATC D06BB10
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Swissmedic (Switzerland)- Active substance
- imiquimodum
- Manufacturer
- Viatris Pharma GmbH
- Country
- Switzerland (CH)
- ATC code
- D06BB10
- ATC class
- Imiquimod
- Swissmedic category
- A
- Reimbursed
- Yes
- Source register
- Swissmedic (Switzerland)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- gtin7680631650022Btl 28 StkCHF 130.05
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
74 interactions on record for imiquimod.
Graded by severity as the source publishes them — 1 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
Imiquimod · interactions on record
74 records
- 1 severe
- 3 moderate
- 70 info
Most severe, free to view
- Aminolevulinic acidL01XD04severe
- Porfimer sodiumL01XD01moderate
- MethoxsalenL01XD10moderate
- VerteporfinS01LA01moderate
- 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
Imiquimod in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesImiquimodAnvi Pharmaceuticals Inc.
- United KingdomAldara 5% cream 250mg sachetsDowelhurst Ltd
- FinlandAldaraViatris Healthcare Limited
- CzechiaALDARAVIATRIS HEALTHCARE LIMITED, Dublin
- SpainALDARA 5% CREMAViatris Healthcare Limited
- CanadaALDARA PBAUSCH HEALTH, CANADA INC.
- FranceALDARA 5 %, crèmeVIATRIS HEALTHCARE (IRLANDE)
- NetherlandsAldara 5% cremeViatris Healthcare Limited
Authorised across Europe · EMA
The same active substance is authorised in 14 EEA countries. Names it is sold under:
- Austria · Imikeraderm
- Cyprus · Modiwart
- Germany · Aksunim, Imikeraderm
- Spain · Imikeraderm, Imunocare
- United Kingdom (Northern Ireland) · Bascellex
- Greece · Modiwart, Quimodia
- Iceland · Aldara, Zyclara
- Italy · Imunocare
- Liechtenstein · Aldara, Zyclara
- Netherlands · Bascellex
- Norway · Aldara, Bascellex
- Poland · Imikeraderm
- Portugal · Imicare
- Sweden · Bascellex
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 Swissmedic (Switzerland). 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/a6052687-8c1a-47fb-b1ec-1dfe61e0da67 GET /v1/drugs/a6052687-8c1a-47fb-b1ec-1dfe61e0da67?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.
{
"unit": null,
"strength": "imiquimodum 37.5 mg",
"valid_from": "2015-03-01",
"limitations": "[{\"description\":\"Zyclara ist angezeigt für die topische Behandlung von klinisch typischer, nicht hyperkeratotischer, nicht hypertropher, sichtbarer oder tastbarer aktinischer Keratose (AK) im Gesicht oder auf der unbehaarten Kopfhaut bei immunkompetenten Erwachsenen, wenn andere topische Behandlungsmöglichkeiten kontraindiziert oder weniger geeignet sind.\",\"costApproval\":null,\"isNew\":false,\"limitationCode\":null,\"priceModel\":null,\"validFrom\":\"2015-03-01\"}]",
"galenic_form": "Creme 37.5 mg/g",
"therapeutic_area": null,
"sl_inclusion_date": "2015-03-01",
"self_retention_pct": 10
}See everything about imiquimod.
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.