Marketing-authorisation holder · United States
EMD Serono, Inc.
23 medicines in 1 country, as authorisation holder.
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Marketing-authorisation holder · United States
23 medicines in 1 country, as authorisation holder.
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Groups are put together by Prognia from the names regulators publish and from company links; they are not an official corporate structure.
Every medicine in the registers under its name, current ones first.
23 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| BAVENCIO20mg/ml · Injectable | Avelumab | United States | Marketed | 2017 |
| BAVENCIO20mg/ml · Injectable | Avelumab | United States | Marketed | 2017 |
| CETROTIDE0.25mg base/vial | 3mg base/vial · Powder | Cetrorelix | United States | Marketed | 2000 |
| EUTHYROX0.025mg | 0.05mg | 0.075mg | 0.088mg | 0.112mg | 0.125mg | 0.137mg | 0.15mg | 0.175mg | 0.1mg | 0.2mg | 0.3mg · Tablet | Levothyroxine | United States | Not marketed | 2002 |
| GEREF0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 0.5MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reason · Injectable | Sermorelin | United States | Not marketed | 1990 |
| GLUCOPHAGE1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 750MG **Federal Register · Tablet | Metformin | United States | Not marketed | 1995 |
| GLUCOPHAGE XR500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended release | Metformin | United States | Not marketed | 2000 |
| GONAL-F1,050 iu/vial | 150 iu/vial | 37.5 iu/vial | 450 iu/vial | 75 iu/vial · Injectable | Follitropin alfa/beta | United States | Marketed | 1997 |
| GONAL-F RFF75 iu/vial · Injectable | Follitropin alfa/beta | United States | Marketed | 2004 |
| GONAL-F RFF REDI-JECT150 iu/0.25ml | 300 iu/0.5ml | 450 iu/0.75ml | 900 iu/1.5ml · Injectable | Follitropin alfa/beta | United States | Marketed | 2004 |
| MAVENCLAD10mg · Tablet | Cladribine | United States | Marketed | 2019 |
| OVIDREL0.25mg /0.5ml · Injectable | Choriogonadotropin alfa | United States | Marketed | 2000 |
| OVIDREL0.25mg/vial · Injectable | Choriogonadotropin alfa | United States | Not marketed | 2000 |
| Rebif22mcg/0.5ml · Injection | Interferon beta-1a | United States | Marketed | 2012 |
| Rebif8.8mcg/0.2ml · Injection | Interferon beta-1a | United States | Marketed | 2004 |
| Rebif44mcg/0.5ml · Injection | Interferon beta-1a | United States | Marketed | 2012 |
| Rebif8.8mcg/0.2ml · Injection | Interferon beta-1a | United States | Marketed | 2012 |
| SAIZEN4mg/vial | 5mg/vial | 6mg/vial | 8.8mg/vial · Injectable | Somatropin | United States | Marketed | 1996 |
| SEROPHENE50mg · Tablet | Clomifene | United States | Not marketed | 1982 |
| SEROSTIM4mg/vial | 5mg/vial | 6mg/vial | 8.8mg/vial · Injectable | Somatropin | United States | Marketed | 1996 |
| SEROSTIM LQ6mg/0.5ml (6mg/0.5ml) · Injectable | Somatropin | United States | Not marketed | 1996 |
| TEPMETKO225mg base · Tablet | Tepotinib | United States | Marketed | 2021 |
| ZORBTIVE4mg/vial | 5mg/vial | 6mg/vial | 8.8mg/vial · Injectable | Somatropin | United States | Marketed | 2003 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 23 | 23 | 0 | 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.
Other companies in the same group.
Ranked by their number of medicines.