Poland· PL-100397017

Rifamycin Adalvo

A antibiotics product containing rifamycinum natricum, registered in Poland by Adalvo Competence Center S.R.L.. The same ATC class is registered in 2 of our 19 countries.

ATC A07AA

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedRifamycin AdalvoATCA07AAREGISTER NO.PL-100397017PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Rifamycinum natricum is registered in 2 of 19 countries.

Countries holding a registration under ATC A07AA (antibiotics), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 2 of them publish a price we can compare per daily dose

Rifamycinum natricum · ATC A07AA

2 / 19 countries

  • Polandprice
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

URPL (Poland)
Active substance
Rifamycinum natricum
Manufacturer
Adalvo Competence Center S.R.L.
Country
Poland (PL)
ATC code
A07AA
ATC class
Antibiotics
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    05909991396473

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Rifamycinum natricum in 7 other countries

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

All rifamycinum natricum products

Authorised across Europe · EMA

The same active substance is authorised in 12 EEA countries. Names it is sold under:

  • Belgium · Rifocine I.V.
  • Bulgaria · Relafalk
  • Germany · Gutivia
  • Finland · Relafalk
  • France · Otofa, Rifamycine Chibret
  • Greece · Relafalk
  • Hungary · Relafalk
  • Italy · Dotecine, Rifocin
  • Luxembourg · Otofa, Rifocine I.V.
  • Norway · Relafalk
  • Portugal · Imfalda, Rifocina
  • Sweden · Relafalk

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 URPL (Poland). 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/b3e4e9c9-1c06-4023-b730-7c2aea863055
GET /v1/drugs/b3e4e9c9-1c06-4023-b730-7c2aea863055?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.

{
  "form": "Tabletki o zmodyfikowanym uwalnianiu",
  "source": "urpl",
  "strength": "200 mg",
  "packaging": "05909991396473 ¦ Rp ¦ 131563\n12 tabl.",
  "substance": "Rifamycin sodium 200 mg",
  "common_name": "Rifamycinum natricum",
  "pl_product_id": "100397017",
  "pozwolenie_nr": "25180",
  "auth_procedure": "DCP",
  "authorisation_validity": "Bezterminowe"
}

See everything about rifamycinum natricum.

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.