Japan· JP-6343456D1024
乾燥濃縮人α1-プロテイナーゼインヒビター
A medicinal product containing 乾燥濃縮人α1-プロテイナーゼインヒビター, registered in Japan by オーファンパシフィック, on the national reimbursement list.
Checked against MHLW / PMDA (Japan) on
Informational only — not a medical device.
The record
At a glance
MHLW / PMDA (Japan)- Active substance
- 乾燥濃縮人α1-プロテイナーゼインヒビター
- Manufacturer
- オーファンパシフィック
- Country
- Japan (JP)
- ATC code
- —
- 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
乾燥濃縮人α1-プロテイナーゼインヒビター in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandProlastinaGrifols Deutschland GmbH
- FranceALFALASTIN 33,33 mg/mL, poudre et solvant pour solution injectableLFB-BIOMEDICAMENTS
- CzechiaPROLASTINAGrifols Deutschland GmbH, Frankfurt
- NorwayProlastinaGrifols Deutschland GmbH
- SwedenProlastina 1000 mg Pulver och vätska till infusionsvätska, lösningGrifols Deutschland GmbH
- PolandRespreezaCSL Behring GmbH
- IrelandProlastin 4000 mg, powder and solvent for solution for infusionGrifols Deutschland GmbH
- IcelandRespreezaCSL Behring GmbH*
Authorised across Europe · EMA
The same active substance is authorised in 21 EEA countries. Names it is sold under:
- Austria · Prolastin
- Belgium · Pulmolast
- Cyprus · Prolastina
- Czechia · Prolastina
- Germany · Prolastin
- Denmark · Prolastina
- Spain · Prolasplan, Prolastina
- Finland · Prolastina
- France · Alfalastin, Prolastin
- Greece · Prolastin
- Croatia · Prolastina
- Ireland · Prolastin
- Iceland · Respreeza
- Italy · Plitalfa, Prolastin
- Liechtenstein · Respreeza
- Netherlands · Prolastin
- Norway · Prolastina, Respreeza
- Poland · Prolastin, Prolastin, 4000 Mg
- Portugal · Prolastin
- Sweden · Prolastina
- Slovakia · Prolastina
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/0f2f554e-1c9b-4a14-9e31-38d4b5cdbb61 GET /v1/drugs/0f2f554e-1c9b-4a14-9e31-38d4b5cdbb61?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": "1,000mg1瓶(溶解液付)",
"marks": null,
"source": "mhlw",
"remarks": null,
"yj_code": "6343456D1024",
"category": "注射薬",
"price_yen": 216054,
"generic_name": "乾燥濃縮人α1-プロテイナーゼインヒビター",
"product_name_jp": null,
"therapeutic_class": "6343",
"transitional_expiry": null
}See everything about 乾燥濃縮人α1-プロテイナーゼインヒビター.
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.