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Sweden· SE-20020328000043

Dynastat 40 mg Pulver och vätska till injektionsvätska, lösning

A medicinal product containing parecoxib, registered in Sweden by Pfizer Europe MA EEIG.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedDynastat 40 mg Pulver och vätska till…ATC—REGISTER NO.SE-20020328000043PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Parecoxib
Manufacturer
Pfizer Europe MA EEIG
Country
Sweden (SE)
ATC code
—
Reimbursed
Not published by this register
Source register
Swedish Medical Products Agency (Sweden)
Last checked
October 1, 2026

Packs & prices · 1

  • se_varunummer
    20020328000043

Regulatory notes

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

Same medicine, other countries

Parecoxib in 12 other countries

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

All parecoxib products

Authorised across Europe · EMA

The same active substance is authorised in 13 EEA countries. Names it is sold under:

  • Germany · Parecoxib Chenpon, Parecoxib Noridem
  • Denmark · Parecoxib Macure, Parecoxib Noridem
  • Finland · Parecoxib Macure
  • United Kingdom (Northern Ireland) · Parecoxib Aspire Pharma, Parecoxib Noridem Enterprises
  • Greece · Coxidem, Pyrixip
  • Ireland · Parecoxib Noridem Enterprises Limited
  • Iceland · Dynastat, Parecoxib Macure
  • Liechtenstein · Dynastat
  • Malta · Parecoxib Noridem
  • Netherlands · Parecoxib Chenpon, Parecoxib Seacross
  • Norway · Dynastat, Parecoxib Macure
  • Portugal · Parecoxib Noridem, Pyrixip
  • Romania · Parecoxib Noridem

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 Swedish Medical Products Agency (Sweden). 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/c8ac0456-a740-4bb3-905c-56be977ad5a7
GET /v1/drugs/c8ac0456-a740-4bb3-905c-56be977ad5a7?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.

{
  "source": "lakemedelsverket",
  "doc_types": [
    "EPAR",
    "EMA"
  ],
  "se_npl_id": "20020328000043",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20020328000043",
  "product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/dynastat-epar-product-information_sv.pdf"
}

See everything about parecoxib.

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.