Group structure
17 companies in 8 countries
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17 companies in 8 countries
One free account for the Prognia apps: Ward to study, Osler for clinical answers with their sources, and the network to find your colleagues.
Groups are put together by Prognia from the names regulators publish and from company links; they are not an official corporate structure.
Every medicine of every company in the group, current ones first.
1–25 of 95
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| ABEVMY400 mg / 16 ml · Solution | Bevacizumab | Canada | Marketed | 2022 |
| ABEVMY100 mg / 4 ml · Solution | Bevacizumab | Canada | Marketed | 2022 |
| ABEVMY | Bevacizumab | Brazil | Authorised | 2025 |
| APIXABAN BIOCONCompressa rivestita con film | Apixaban | Italy | Authorised | |
| Apixaban Biocon 2,5 mg filmomhulde tablettenFilmomhulde tablet | Apixaban | Netherlands | Authorised | 2025 |
| Apixaban Biocon 5 mg filmomhulde tablettenFilmomhulde tablet | Apixaban | Netherlands | Authorised | 2025 |
| AUKELSO120mg/1.7ml(70mg/ml) · Injectable | Denosumab | United States | Marketed | 2025 |
| BOSAYA | Denosumab | Brazil | Authorised | 2026 |
| BOSAYA60 mg / ml · Solution | Denosumab | Canada | Authorised | |
| BOSAYA60mg/ml · Injectable | Denosumab | United States | Marketed | 2025 |
| Dabigatran etexilaat Biocon 110 mg harde capsulesCapsule, hard | Dabigatran etexilate | Netherlands | Authorised | 2024 |
| Dabigatran etexilaat Biocon 150 mg harde capsulesCapsule, hard | Dabigatran etexilate | Netherlands | Authorised | 2024 |
| Dabigatran etexilaat Biocon 75 mg harde capsulesCapsule, hard | Dabigatran etexilate | Netherlands | Authorised | 2024 |
| DABIGATRAN ETEXILATO BIOCONCapsula rigida | Dabigatran etexilate | Italy | Authorised | |
| DIAVORINSoluzione iniettabile in penna pre-riempita | Liraglutide | Italy | Authorised | |
| Diavorin 6 mg/ml oplossing voor injectie in een voorgevulde penOplossing voor injectie | Liraglutide | Netherlands | Authorised | 2025 |
| DIAVORIN 6 MG/ML SOLUCION INYECTABLE EN PLUMA PRECARGADA6 mg · Solución inyectable en pluma precargada | Liraglutide | Spain | Authorised | 2026 |
| Dimethylfumaraat Biocon 120 mg, harde maagsapresistente capsulesMaagsapresistente capsule, hard | Dimethyl | Netherlands | Authorised | 2025 |
| Dimethylfumaraat Biocon 240 mg, harde maagsapresistente capsulesMaagsapresistente capsule, hard | Dimethyl | Netherlands | Authorised | 2025 |
| DIMETILFUMARATO BIOCONCapsula rigida gastroresistente | Dimethyl | Italy | Authorised | |
| EVEROLIMUS BIOCONCompressa | Everolimus | Italy | Authorised | |
| EVEROLIMUS BIOCON 10 MG COMPRIMIDOS EFG10 mg · Comprimido | Everolimus | Spain | Authorised | 2022 |
| Everolimus Biocon 10 mg tablettenTablet | Everolimus | Netherlands | Authorised | 2021 |
| EVEROLIMUS BIOCON 2,5 MG COMPRIMIDOS EFG2,5 mg · Comprimido | Everolimus | Spain | Authorised | 2022 |
| Everolimus Biocon 2,5 mg tablettenTablet | Everolimus | Netherlands | Authorised | 2021 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 22 | 18 | 4 | CompaniesAll medicines |
| Canada | 21 | 21 | 0 | CompaniesAll medicines |
| Netherlands | 20 | 20 | 0 | CompaniesAll medicines |
| Brazil | 12 | 12 | 0 | CompaniesAll medicines |
| Italy | 8 | 8 | 0 | CompaniesAll medicines |
| Saudi Arabia | 7 | 7 | 0 | CompaniesAll medicines |
| Spain | 5 | 5 | 0 | CompaniesAll medicines |
Also in the registers of Singapore, United Kingdom
The ATC groups most of its medicines belong to, largest first.
The active substances in most of its medicines.
How the registers spell it, normalised: legal forms, accents and capitals removed.
Compiled by Prognia from the public medicine and company registers below. Logos are not used.
Companies are grouped by Prognia from the names regulators publish; not an official corporate structure.
Fuente de la información: AEMPS (CIMA).
Licence: AEMPS open data reuse with attribution
Source: U.S. FDA, Drugs@FDA / openFDA. FDA does not endorse this site.
Licence: Public domain (U.S. Government work)
ANVISA / CMED, consumer price table; embedded source date 2026-07-21 and retrieval date
Licence: Other (Public Domain)
Anvisa published factual open-data CSV https://dados.anvisa.gov.br/dados/CONSULTAS/PRODUTOS/TA_CONSULTA_MEDICAMENTOS.CSV, HTTP version Mon, 12 Oct 2026 11:45:25 GMT; acquired 12 October 2026; original source states and timestamps retained.
Licence: Brazil federal factual open data, consolidated Decreto 8777/2016 article 4; attribution and third-party exceptions
Anvisa, official medicine/API manufacturer factual export, HTTP source version Fri, 09 Oct 2026 08:21:54 GMT, acquired 2026-10-09; exact unmodified native identifiers and fields preserved.
Licence: Brazil federal factual open-data reuse; Decreto 8777/2016 consolidated article 4 and third-party exceptions
Health Canada, Drug Product Database, company API, entire response observed 2026-10-10T15:12:05.508784+00:00; native facts projected by Prognia.
Licence: Open Government Licence Canada
Health Canada, Drug Product Database, drugproduct API, entire response observed 2026-10-10T15:12:07.336870+00:00; native facts projected by Prognia.
Licence: Open Government Licence Canada
Fuente de la información: Agencia Española de Medicamentos y Productos Sanitarios www.aemps.gob.es; CIMA presentaciones, acquired 11 October 2026 UTC; each source response/update date retained.
Licence: AEMPS explicit public open-data reuse for citizens and companies; source attribution and update date required
Fuente de la información: Agencia Española de Medicamentos y Productos Sanitarios www.aemps.gob.es; CIMA medicamentos, acquired 11 October 2026 UTC; each source response/update date retained.
Licence: AEMPS explicit public open-data reuse for citizens and companies; source attribution and update date required
Medicines and Healthcare products Regulatory Agency (MHRA), GOV.UK; Category 1 list; publication updated 25 August 2026; acquired 2026-10-15T08:18:47.757811+00:00; original workbook cells and factual authorization/holder projections adapted under Open Government Licence v3.0.
Licence: Open Government Licence v3.0; exact Crown copyright 2026 publication grant
Medicines and Healthcare products Regulatory Agency (MHRA), GOV.UK; Category 2 list; publication updated 25 August 2026; acquired 2026-10-15T08:18:48.423930+00:00; original workbook cells and factual authorization/holder projections adapted under Open Government Licence v3.0.
Licence: Open Government Licence v3.0; exact Crown copyright 2026 publication grant
Report an error or request removalCorrections from the company itself are welcome.
Contains Irish Public Sector Data licensed under Creative Commons Attribution 4.0 International (CC BY 4.0), Companies Registration Office; original dataset/API URL and company number, exact locator/source version and retrieval date; selected field normalization by Prognia. https://creativecommons.org/licenses/by/4.0/
Licence: Creative Commons Attribution
Agenzia Italiana del Farmaco (AIFA); https://drive.aifa.gov.it/farmaci/confezioni_fornitura.csv; HTTP Last-Modified Mon, 12 Oct 2026 23:02:44 GMT; acquired 2026-10-13T17:21:16.224007+00:00; native fields retained, source identifier and role projections are adaptations.
Licence: CC BY 4.0; AIFA published open-data catalog
College ter Beoordeling van Geneesmiddelen, Geneesmiddeleninformatiebank metadata, source update 07-10-2026; downloaded 08-10-2026; factual adaptation.
Licence: Conditional noncreative administrative factual metadata; no dataset-wide CC0 claim
Saudi Food and Drug Authority (SFDA), foreign human medicine open-data listing, source scope 2023, retrieved 11 October 2026 UTC; exact original file and response modification date retained.
Licence: Exact SFDA open-data section explicitly offers freely usable named human medicine workbooks; factual-data scope only
Contains information from HSA Listing of Registered Therapeutic Products accessed on 8 October 2026 from data.gov.sg, under Singapore Open Data Licence 1.0: https://data.gov.sg/open-data-licence
Licence: Singapore Open Data Licence
FDA Purple Book, September 2026 release; acquired 2026-10-10T15:29:54.330165+00:00; exact source fields retained with source-key projections.
Licence: FDA-created structured factual administrative metadata; public-domain policy with third-party exceptions