Mundipharma Regulatory GmbH

Mundipharma Regulatory GmbH is recorded by Swissmedic as the authorisation holder for 8 human medicines, which places it 170 of 334 authorisation holders. Its portfolio is mostly in the Synthetika category (100 % of its authorisations). We hold no research of our own on this company's sector or business model, so we assign it to none.

Sector unverified: the Swissmedic list carries no sector field and we have not researched this company.

Key facts

SectorNot available
CityNot available
CantonNot available
Authorisation holderYes
Medicines8
FoundedNot available
EmployeesNot available
Parent groupNot available
ActivityNot available
WebsiteNot available

Medicines authorised in Switzerland

Mundipharma Regulatory GmbH is recorded by Swissmedic as the authorisation holder for 8 human medicines. The table shows 8 of them with product code and dispensing category.

Portfolio by product code

  • Synthetika8

Portfolio by dispensing category

  • A+8

8 of 8 authorisations

NameAuthorisation numberDispensing categoryATCFirst authorised
Hydromorphone Mundipharma 1.3 mg70346A+N02AA032025-07-18
Hydromorphone Mundipharma 2 mg70222A+N02AA032025-04-16
Hydromorphone Mundipharma Retard 4 mg70347A+N02AA032025-07-18
Morphine Mundipharma 30 mg69352A+-2023-05-17
Oxycodone Mundipharma 10 mg69353A+-2023-05-26
Oxycodone Mundipharma 10 mg/1 ml69354A+-2023-05-10
Oxycodone Mundipharma 5 mg69424A+-2023-08-11
Oxycodone/Naloxone Mundipharma 10 mg/5 mg69358A+-2023-05-17

Frequently asked questions

How many medicines does Mundipharma Regulatory GmbH have authorised in Switzerland?

Mundipharma Regulatory GmbH is recorded by Swissmedic as the authorisation holder for 8 human medicines (as of 1 September 2026). Different strengths under one authorisation number are not counted separately.

Where is Mundipharma Regulatory GmbH based?

We have no confirmed Swiss address for Mundipharma Regulatory GmbH. We add it as soon as the commercial register or the company confirms it.

Is Mundipharma Regulatory GmbH a Swissmedic authorisation holder?

Yes. Mundipharma Regulatory GmbH appears in the official Swissmedic list of authorised medicinal products as an authorisation holder. Under the Therapeutic Products Act (TPA) the holder is responsible for the quality, safety and product information of its medicines in Switzerland.

Sources

Last updated:

Data from the Swissmedic list of authorised medicinal products as of 1 September 2026. We hold no research of our own on this company's location, sector or website.

About the operator

Swiss Pharma Partners

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