Marketing-authorisation holder · United States
Sanofi-Aventis U.S. LLC
9 medicines in 1 country, as authorisation holder and manufacturer.
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Marketing-authorisation holder · United States
9 medicines in 1 country, as authorisation holder and manufacturer.
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Every medicine in the registers under its name, current ones first.
9 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| Elitek7.5mg · For Injection | Rasburicase | United States | Marketed | 2006 |
| Kevzara200mg/1.14ml · Injection | Sarilumab | United States | Marketed | 2018 |
| Kevzara150mg/1.14ml · Injection | Sarilumab | United States | Marketed | 2018 |
| Lantus300units/3ml (100units/ml) · Injection | Insulin glargine | United States | Not marketed | 2000 |
| Lantus500units/5ml (100units/ml) · Injection | Insulin glargine | United States | Not marketed | 2000 |
| MERILOG10ml(100units/ml) · Injection | Insulin aspart | United States | Marketed | 2025 |
| MERILOG SOLOSTAR3ml(100units/ml) · Injection | Insulin aspart | United States | Marketed | 2025 |
| Sarclisa Escena1,400mg/10ml (140mg/ml) · Injection | Isatuximab | United States | Marketed | 2026 |
| Zaltrap200mg/8ml (25mg/ml) · Injection | Ziv-aflibercept | United States | Marketed | 2012 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 9 | 9 | 0 | CompaniesAll medicines |
Also in the registers of Brazil
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)
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
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.