Private company

Gedeon Richter Ltd.

Logo: Tothfanni gedeonrichter, CC BY-SA 4.0, via Wikimedia Commons3

Hungarian pharmaceutical company

Gedeon Richter Plc. is a Hungarian multinational pharmaceutical and biotechnology company headquartered in Budapest. Founded in 1901 by pharmacist Gedeon Richter, it is listed on the Budapest Stock Exchange under the ticker symbol RICHTER and is a constituent of the BUX Index.2 It employed about 12,700 people in 2018.1 Its revenue was €1.4 billion in 2018.1 Wikipedia text CC BY-SA 4.0

Last updated Oct 21, 2026.

Overview

1901Founded1
Richter-Gedeon-Nyrt-P5010610
Photo: The original uploader was Misibacsi at Hungarian Wikipedia ., CC BY-SA 3.0, via Wikimedia Commons5

Gedeon Richter Plc. is a Hungarian multinational pharmaceutical and biotechnology company headquartered in Budapest. Founded in 1901 by pharmacist Gedeon Richter, it is listed on the Budapest Stock Exchange under the ticker symbol RICHTER and is a constituent of the BUX Index.2

The story

Founded by Gedeon Richter in 1901.1

Early history

In 1901, the pharmacist Gedeon Richter founded the company, when he first received a license to industrially produce medicines.

Initially, small-scale pharmaceutical production took place in the Arany Sas (Golden Eagle) Pharmacy, which still operates today. At the time pharmaceutical production on an industrial scale required heavy investments, and large-scale pharmaceutical manufacturing activities were considered to be extremely capital-intensive operations. Initially, the laboratory processed extracts from organs of animals and produced organotherapeutic drugs.

The plant was built in 1907 in the Kőbánya suburb of Budapest and was Hungary's first pharmaceutical manufacturing plant and regarded as an outstanding technological achievement in its day. In compliance with the established international trends of the pharmaceutical industry in those days, the company produced herbal drugs, processed extracts from plants and manufactured synthetic products at a later date. The company became a highly recognized manufacturer of lecithin products, antiseptics (Hyperol), as well as brands of Aspirin, and adrenalin, which continue to be in use. In 1934, Constant Janssen, of the future Janssen Pharmaceuticals, acquired the distribution rights for Gedeon Richter's products.

The company was nationalized in 1948 and remained fully state-owned until 1994.

In the 1970s, chemists at the Gedeon Richter Chemical Works in Budapest discovered the brain enhancing drug vinpocetine,. This drug was introduced to the market in 1977 and became its most successful new product, marketed as Cavinton for treament for cerebrovascular disorders such as stroke and dementia.

In 1995 Gedeon Richter signed a contract with Danco Laboratories to market an abortion pill mifepristone in the US. Danco resolved to contracting Gedeon, because its prior attempts to find a US distributor failed due to "the politically volatile climate surrounding abortion in this country [the USA]." Facing a strong opposition from the US pro-life groups, Gedeon decided in 1997 to end its efforts to place mifepristone on the U.S. market. On May 9, 1997 Danco filed a lawsuit against Gedeon, because they lost over $200 million due to the Gedeon's breach of contract.

Recent history

In May 2006 Gedeon Richter signed a development and supply agreement with the US-based company Repros Therapeutics to produce Proellex. In July 2007 Gedeon Richter signed a contract with Barr Pharma for the production of terbinafine, originally Novartis' Lamisil, where Barr paid Gedeon Richter a royalty for distributing the product in the U.S.

From July 2008 - April 2012, the company constructed a new manufacturing facility ($110 million) in Debrecen.

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In October 2010, Gedeon Richter acquired 100% of a private Swiss biopharmaceutical company, PregLem, for CHF 445 million (€337 million). PregLem is focused on the treatment of gynecological conditions and infertility.

In 2015, Stada Arzneimittel AG and Gedeon Richter signed a license and distribution agreement to commercialize Richter's biosimilar Pegfilgrastim in Europe. According to the agreement Stada receives non-exclusive distribution rights for the area of geographical Europe (excluding Russia), while Richter retains its rights to distribute and market biosimilar Pegfilgrastim worldwide.

In January 2017, William de Gelsey resigned as chairman of Gedeon Richter. He was replaced by former CEO Erik Bogsch, who was chief executive officer of Gedeon Richter from 1992 to November 2017. As the new CEO he appointed Gabor Orban, a former fund manager, government official and Bogsch's deputy since 2016. De Gelsey remained a board member until his death.

In April 2017, Evestra signed a collaboration partnership agreement with Gedeon Richter. In February 2019, Gedeon Richter and Pantarhei Bioscience signed a license and supply agreement for the commercialization of a novel combined oral contraceptive.

In September 2018 the company started collaborating with the company Mithra Pharmaceuticals to distribute its contraceptive, Estelle, in Europe and Russia.

Richter's atypical antipsychotic, Reagila, containing the active ingredient cariprazine, was awarded the prize of Medicine of the Year 2019 by the Hungarian Society for Experimental and Clinical Pharmacology (MFT).

From Wikipedia’s article on Gedeon Richter (company), shared under CC BY-SA 4.0.4

Leadership

Who has led Gedeon Richter Ltd., and when. Pick a name to see everywhere that person has worked.

Products and brands

  • medication

Listed on Wikidata.1

Employees over time

  • 201812,6961

Revenue over time

As stated on Wikidata, in the currency reported.

Revenue

  • 20181.4B EUR1

Net income

  • 2018112.8M EUR1

Timeline

  1. 1901Founded Founded1

Calendar

Drug trials and FDA: coming up

  1. Dec 15, 2026Phase 3 trial readout expected Phase 3 trial of Cariprazine in Schizophrenia: primary completion expected Dec 15, 2026 (ClinicalTrials.gov NCT03817502).6

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). Trials from ClinicalTrials.gov, as the sponsor registered them (expected dates are the sponsor's own and often move); approvals and advisory committee meetings from the FDA. The FDA does not publish its decision (PDUFA) dates. The full markets calendar