Marketing-authorisation holder · United States
Biogen Inc.
15 medicines in 1 country, as authorisation holder.
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Marketing-authorisation holder · United States
15 medicines in 1 country, as authorisation holder.
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Every medicine in the registers under its name, current ones first.
15 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| ADUHELM170mg/1.7ml (100mg/ml) | 300mg/3ml (100mg/ml) · Injectable | Aducanumab | United States | Marketed | 2021 |
| Avonex30mcg/0.5ml · Injection | Interferon beta-1a | United States | Marketed | 2012 |
| AVONEX1a 30ug/ml · Vial | Interferon beta-1a | United States | Marketed | 1996 |
| Avonex30mcg/0.5ml · Injection | Interferon beta-1a | United States | Marketed | 2003 |
| Plegridy94mcg/0.5ml · Injection | Peginterferon beta-1a | United States | Marketed | 2014 |
| Plegridy94mcg/0.5ml · Injection | Peginterferon beta-1a | United States | Marketed | 2014 |
| Plegridy63mcg/0.5ml · Injection | Peginterferon beta-1a | United States | Marketed | 2014 |
| Plegridy125mcg/0.5ml · Injection | Peginterferon beta-1a | United States | Marketed | 2014 |
| Plegridy63mcg/0.5ml · Injection | Peginterferon beta-1a | United States | Marketed | 2014 |
| SKYCLARYS50mg · Capsule | Omaveloxolone | United States | Marketed | 2023 |
| TECFIDERA120mg | 240mg · Capsule, delayed release | Dimethyl | United States | Marketed | 2013 |
| VUMERITY231mg · Capsule, delayed release | Diroximel fumarate | United States | Marketed | 2019 |
| ZINBRYTA150mg/ml · Injectable | Daclizumab | United States | Marketed | 2016 |
| ZURZUVAE20mg | 25mg | 30mg · Capsule | Zuranolone | United States | Marketed | 2023 |
| Zinbryta150mg/ml · Injection | Daclizumab | United States | Withdrawn | 2017 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 15 | 14 | 1 | CompaniesAll medicines |
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.
Source: U.S. FDA, Drugs@FDA / openFDA. FDA does not endorse this site.
Licence: Public domain (U.S. Government work)
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
Report an error or request removalCorrections from the company itself are welcome.
Ranked by their number of medicines.