United Kingdom· GB-APID-28357211000001106
Duaklir 340micrograms/dose / 12micrograms/dose Genuair
A medicinal product containing aclidinium bromide + formoterol, registered in United Kingdom by Covis Pharma GmbH.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Aclidinium bromide + Formoterol
- Manufacturer
- Covis Pharma GmbH
- Country
- United Kingdom (GB)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 5
- gtin05000456008396
- gtin08719992718023
- gtin8719992718023
- gtin5000456008396
- gtin8430308130093
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Aclidinium bromide + formoterol in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaBRIMICA GENUAIRCovis Pharma Europe B.V., Amsterdam
- SpainBRIMICA GENUAIR 340 MICROGRAMOS/12 MICROGRAMOS POLVO PARA INHALACIONCovis Pharma Europe B.V.
- SwedenBrimica Genuair 340 mikrogram/12 mikrogram InhalationspulverCovis Pharma Europe B.V.
- IcelandBrimica GenuairCovis Pharma Europe B.V.
- NetherlandsBrimica Genuair 340 microgram/12 microgram, inhalatiepoederCovis Pharma Europe B.V.
- FinlandBrimica GenuairCOVIS PHARMA EUROPE B.V.
- PolandBrimica GenuairCovis Pharma Europe B.V.
- United StatesDUAKLIR PRESSAIRCovis Pharma US, Inc
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Brimica Genuair, Duaklir Genuair
- Liechtenstein · Brimica Genuair, Duaklir Genuair
- Norway · Brimica Genuair, Duaklir Genuair
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 NHS dm+d (United Kingdom). 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/30e0d891-ccac-4a74-a980-a858014a60ae GET /v1/drugs/30e0d891-ccac-4a74-a980-a858014a60ae?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.
{
"apid": "28357211000001106",
"desc": "Duaklir 340micrograms/dose / 12micrograms/dose Genuair (Covis Pharma GmbH)",
"form": "Inhalation powder",
"vpid": "28365011000001100",
"source": "dmd",
"vtm_id": "28367211000001102",
"strength": "11.8 microgram",
"substance": "Aclidinium bromide + Formoterol",
"ingredient": "Formoterol fumarate dihydrate",
"supplier_code": "42474411000001102"
}See everything about aclidinium bromide + formoterol.
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.