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Japan· JP-4490409G2029

トラロキヌマブ(遺伝子組換え)

A tralokinumab product containing トラロキヌマブ(遺伝子組換え), registered in Japan by レオファーマ, on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

On Japan’s NHI price listATC D11AH07

Checked against MHLW / PMDA (Japan) on

Informational only — not a medical device.

SOURCE REGISTER · JPMHLW / PMDA (Japan)normalisedトラロキヌマブ(遺伝子組換え)ATCD11AH07REGISTER NO.JP-4490409G2029PACKS LISTED0CHECKEDSeptember 25, 2026

Where it is registered

Tralokinumab is registered in 14 of 19 countries.

Countries holding a registration under ATC D11AH07 (tralokinumab), each read from that country’s own register.

  • This record: Japan, from MHLW / PMDA (Japan)
  • 8 of them publish a price we can compare per daily dose

Tralokinumab · ATC D11AH07

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • 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.

Price per daily dose

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

Normalised to the WHO defined daily dose (16.1 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

Tralokinumab · price per daily dose (16.1 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$34.49
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

MHLW / PMDA (Japan)
Active substance
トラロキヌマブ(遺伝子組換え)
Manufacturer
レオファーマ
Country
Japan (JP)
ATC code
D11AH07
ATC class
Tralokinumab
Defined daily dose
16.1 mg, P
Reimbursed
Yes
Source register
MHLW / PMDA (Japan)
Last checked
September 25, 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.

Same medicine, other countries

Tralokinumab in 14 other countries

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

All tralokinumab products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Adtralza
  • Iceland · Adtralza
  • Liechtenstein · Adtralza
  • Norway · Adtralza

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 MHLW / PMDA (Japan). 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/fd144db9-4ee4-4d77-834a-94633dba1494
GET /v1/drugs/fd144db9-4ee4-4d77-834a-94633dba1494?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.

{
  "spec": "300mg2mL1キット",
  "marks": null,
  "source": "mhlw",
  "remarks": null,
  "yj_code": "4490409G2029",
  "category": "注射薬",
  "price_yen": 41859,
  "generic_name": "トラロキヌマブ(遺伝子組換え)",
  "product_name_jp": null,
  "therapeutic_class": "4490",
  "transitional_expiry": null
}

See everything about tralokinumab.

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.