Germany· DE-A57-3e99d283321adaaa
Dalbavancin Accord
A dalbavancin product containing dalbavancin, registered in Germany by Accord Healthcare B.V.. The same ATC class is registered in 16 of our 19 countries.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
Where it is registered
Dalbavancin is registered in 16 of 19 countries.
Countries holding a registration under ATC J01XA04 (dalbavancin), each read from that country’s own register.
- This record: Germany, from EMA Article 57 (European Union)
- 9 of them publish a price we can compare per daily dose
Dalbavancin · ATC J01XA04
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Sweden
- United Kingdom
- United Statesprice
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Dalbavancin
- Manufacturer
- Accord Healthcare B.V.
- Country
- Germany (DE)
- ATC code
- J01XA04
- ATC class
- Dalbavancin
- Defined daily dose
- 1.5 g, P
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
7 interactions on record for dalbavancin.
Graded by severity as the source publishes them — 7 moderate. 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
Dalbavancin · interactions on record
7 records
- 7 moderate
Most severe, free to view
- Sodium picosulfateA06AB08moderate
- Levonorgestrel and ethinylestradiolG03AA07moderate
- Desogestrel and ethinylestradiolG03AA09moderate
- Drospirenone and ethinylestradiolG03AA12moderate
- 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
Dalbavancin in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainDALBAVANCINA ACCORD 500 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSION EFGAccord Healthcare S.L.U.
- SwedenDalbavancin Accord 500 mg Pulver till koncentrat till infusionsvätska, lösningAccord Healthcare B.V.
- United KingdomDalbavancin 500mg powder for concentrate for solution for infusion vialsZentiva Pharma UK Ltd
- FranceDALBAVANCINE ACCORD 500 mg, poudre pour solution à diluer pour perfusionACCORD HEALTHCARE FRANCE
- PolandDalbavancin AccordAccord Healthcare Polska Sp. z o.o.
- NetherlandsDalbavancine Baxter 500 mg poeder voor concentraat voor oplossing voor infusieBaxter B.V.
- IrelandXydalbaAbbVie Deutschland GmbH & Co. KG
- FinlandXydalbaAbbVie Deutschland GmbH&Co.KG
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Dalbavancin, Dalbavancin Accord
- Denmark · Dalbavancin Adalvo, Dalbavancin Teva
- Spain · Dalbavancin Dr. Reddys, Dalbavancina Accord
- Finland · Dalbavancin Adalvo, Dalbavancin Tillomed
- France · Dalbavancine Accord, Dalbavancine Reddy Pharma
- United Kingdom (Northern Ireland) · Dalbavancin Accord, Dalbavancin Reig Jofre Uk
- Greece · Bavalda, Dalbavancin Accord
- Iceland · Xydalba
- Italy · Dalbavancina Accord, Dalbavancina Dr. Reddy’s
- Liechtenstein · Xydalba
- Malta · Bavalda, Dalbavancin Adalvo
- Norway · Dalbavancin Tillomed, Xydalba
- Poland · Dalbavancin Accord, Dalbavancin Reig Jofre
- Portugal · Dalbavancina Anfarm
- Sweden · Dalbavancin Accord, Dalbavancin Bioglan
- Slovakia · Dalbavancin Adalvo
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 EMA Article 57 (European Union). 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/d8f62313-72f9-492e-a95f-667d5406e680 GET /v1/drugs/d8f62313-72f9-492e-a95f-667d5406e680?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.
{
"pzn": null,
"route": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Dalbavancin",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about dalbavancin.
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.