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Poland· PL-100313919

Vipidia

A alogliptin product containing alogliptinum, registered in Poland by Takeda Pharma A/S. The same ATC class is registered in 13 of our 19 countries.

ATC A10BH04

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedVipidiaATCA10BH04REGISTER NO.PL-100313919PACKS LISTED0CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about alogliptinumAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Alogliptin is registered in 13 of 19 countries.

Countries holding a registration under ATC A10BH04 (alogliptin), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 6 of them publish a price we can compare per daily dose
Search alogliptin products by name

Alogliptin · ATC A10BH04

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Germany
  • Icelandprice
  • Ireland
  • Italyprice
  • Japan
  • Netherlands
  • Polandprice
  • United Kingdom
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.

Price per daily dose

What a daily dose of alogliptin costs, country by country.

Normalised to the WHO defined daily dose (25 mg), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown
Open the full comparison — free accountDrug prices for market access

Alogliptin · price per daily dose (25 mg)

USD · FX 28 Sept 2026

  • IT Italy$4.54
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

URPL (Poland)
Active substance
Alogliptinum
Manufacturer
Takeda Pharma A/S
Country
Poland (PL)
ATC code
A10BH04
ATC class
Alogliptin
Defined daily dose
25 mg, O
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 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

312 interactions on record for alogliptin.

Graded by severity as the source publishes them — 3 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
Check alogliptin against other medicinesHow interaction checks work

Alogliptin · interactions on record

312 records

  • 3 severe
  • 269 moderate
  • 40 minor

Most severe, free to view

  • GatifloxacinJ01MA16severe
  • SucralfateA02BX02moderate
  • ThiethylperazinA04AB03moderate
  • TriflupromazinA04AD06moderate
  • 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

Alogliptin in 9 other countries

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

All alogliptin products

Authorised across Europe · EMA

The same active substance is authorised in 6 EEA countries. Names it is sold under:

  • Germany · Alogliptin Heumann
  • United Kingdom (Northern Ireland) · Alogliptin Aspire Pharma, Alogliptin Torrent
  • Iceland · Vipidia
  • Liechtenstein · Vipidia
  • Malta · Alogliptin Torrent
  • Norway · Vipidia

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/0f2b4776-7316-4e4b-92bd-854881e45bb3
GET /v1/drugs/0f2b4776-7316-4e4b-92bd-854881e45bb3?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 powlekane",
  "source": "urpl",
  "strength": "6,25 mg",
  "packaging": "Rp ¦ EU/1/13/844/001 ¦ 90616\n10 tabl.\nRp ¦ EU/1/13/844/002 ¦ 90617\n14 tabl.\nRp ¦ EU/1/13/844/003 ¦ 90618\n28 tabl.\nRp ¦ EU/1/13/844/004 ¦ 90619\n30 tabl.\nRp ¦ EU/1/13/844/005 ¦ 90620\n56 tabl.\nRp ¦ EU/1/13/844/006 ¦ 90621\n60 tabl.\nRp ¦ EU/1/13/844/007 ¦ 90622\n90 tabl.\nRp ¦ EU/1/13/844/008 ¦ 90623\n98 tabl.\nRp ¦ EU/1/13/844/009 ¦ 90624\n100 tabl.",
  "substance": "Alogliptinum 6.25 mg",
  "common_name": "Alogliptinum",
  "pl_product_id": "100313919",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}
API referenceMCP serverPlans

See everything about alogliptin.

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.

Try it freeOpen in the console