Canada· CA-DIN-02329727

DRAXIMAGE DTPA

A medicinal product containing pentetic acid, registered in Canada by JUBILANT DRAXIMAGE INC. DBA JUBILANT RADIOPHARMA.

Checked against Health Canada Drug Product Database (Canada) on

Informational only — not a medical device.

SOURCE REGISTER · CAHealth Canada Drug Product Database (Ca…normalisedDRAXIMAGE DTPAATC—REGISTER NO.CA-DIN-02329727PACKS LISTED0CHECKEDOctober 1, 2026

The record

At a glance

Health Canada Drug Product Database (Canada)
Active substance
PENTETIC ACID
Manufacturer
JUBILANT DRAXIMAGE INC. DBA JUBILANT RADIOPHARMA
Country
Canada (CA)
ATC code
—
Reimbursed
Not published by this register
Source register
Health Canada Drug Product Database (Canada)
Last checked
October 1, 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

Pentetic acid in 9 other countries

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

All pentetic acid products

Authorised across Europe · EMA

The same active substance is authorised in 17 EEA countries. Names it is sold under:

  • Austria · Technescan Dtpa
  • Belgium · Technescan Dtpa
  • Czechia · Technescan Dtpa
  • Germany · Technescan Dtpa
  • Denmark · Technescan Dtpa
  • Spain · Dtpa Technescan
  • Finland · Technescan Dtpa
  • France · Technescan Dtpa
  • United Kingdom (Northern Ireland) · Technescan Dtpa
  • Greece · Technescan Dtpa
  • Hungary · Dtpa Izotóp Intézet, Renon
  • Ireland · Technescan Dtpa
  • Italy · Technescan Dtpa
  • Netherlands · Technescan Dtpa
  • Portugal · Technescan Dtpa
  • Sweden · Technescan Dtpa
  • Slovakia · Technescan Dtpa

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 Health Canada Drug Product Database (Canada). 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/c9d049f1-4c0f-4cee-9410-3d09e47f285c
GET /v1/drugs/c9d049f1-4c0f-4cee-9410-3d09e47f285c?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.

{
  "din": "02329727",
  "form": "POWDER FOR SOLUTION",
  "class": "Radiopharmaceutical",
  "routes": [
    "INTRAVENOUS",
    "INHALATION"
  ],
  "source": "health_canada_dpd",
  "status": "MARKETED",
  "atc_raw": null,
  "schedule": [
    "Schedule C"
  ],
  "drug_code": "81544",
  "strengths": [
    "20 MG"
  ],
  "ahfs_class": null,
  "substances": [
    "PENTETIC ACID"
  ],
  "product_categorization": null
}

See everything about pentetic acid.

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.