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Germany· DE-A57-c45f13966db9038a

Solutio Hydroxychinolini Pharmachem

A oxyquinoline product containing oxyquinoline, registered in Germany by Pharmachem Gmbh & Co. Kg.

ATC D08AH03

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedSolutio Hydroxychinolini PharmachemATCD08AH03REGISTER NO.DE-A57-c45f13966db903…PACKS LISTED0CHECKEDSeptember 30, 2026

The record

At a glance

EMA Article 57 (European Union)
Active substance
Oxyquinoline
Manufacturer
Pharmachem Gmbh & Co. Kg
Country
Germany (DE)
ATC code
D08AH03
ATC class
Oxyquinoline
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

1 interaction on record for oxyquinoline.

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

Oxyquinoline · interactions on record

1 record

  • 1 severe

Most severe, free to view

  • VigabatrinN03AG04severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Oxyquinoline in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All oxyquinoline products

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/14092659-e888-4e38-bf60-d0496e5bbb98
GET /v1/drugs/14092659-e888-4e38-bf60-d0496e5bbb98?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": "Cutaneous Use",
  "source": "ema_art57_de",
  "ma_number": null,
  "substance": "Oxyquinoline",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}

See everything about oxyquinoline.

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.