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Last €83.83 EUR
Change Today -0.18 / -0.21%
Volume 1.7M
SAN On Other Exchanges
EN Paris
EN Paris
New York
As of 11:35 AM 11/27/15 All times are local (Market data is delayed by at least 15 minutes).

sanofi (SAN) Snapshot

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52 Week High
08/6/15 - €101.10
52 Week Low
12/16/14 - €69.77
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Current Stock Chart for SANOFI (SAN)

sanofi (SAN) Details

Sanofi researches, develops, and markets various therapeutic solutions. Its products comprise diabetes solutions, including Lantus, Apidra, and Insuman that are human insulin analogs; Amaryl, an oral sulfonylurea; Lyxumia, a glucagon-like peptide-1 receptor agonist; and Afrezza, an inhaled insulin to improve glycemic control, as well as Toujeo, an insulin glargine. The company also offers Cerezyme to treat gaucher disease; Myozyme/Lumizyme for the pompe disease treatment; Fabrazyme for fabry disease treatment; and Aldurazyme to treat mucopolysaccharidosis type I, as well as provides Aubagio and Lemtrada for multiple sclerosis. In addition, it provides Jevtana for prostate cancer; Taxotere for the treatment of breast, non-small cell lung, prostate, gastric, and head and neck cancers; Thymoglobulin to treat acute rejection in organ transplantation, aplastic anemia, and graft-versus-host diseases; Eloxatin for colorectal cancer; Mozobil for treating hematologic malignancies; and Zaltrap for oxaliplatin resistant metastatic colorectal cancer. Further, the company offers other prescription drugs, such as Plavix for atherothrombosis and acute coronary syndrome; Lovenox for the treatment and prevention of deep vein thrombosis and acute coronary syndromes; Aprovel/CoAprovel for hypertension; Renagel/Renvela to treat chronic kidney disease; Depakine for epilepsy; Synvisc/Synvisc-One for the treatment of pain associated with osteoarthritis of the knee; Stilnox/Ambien/Myslee to treat sleep disorders; Multaq for atrial fibrillation; Allegra for the treatment of allergic rhinitis and urticarial; Actonel for osteoporosis and paget's disease; and Auvi-Q/Allerject for the treatment of severe allergic reactions. Additionally, it offers consumer health care products and generic medicines; and vaccine and animal health products. The company was formerly known as Sanofi-Aventis and changed its name to Sanofi in May 2011. Sanofi was founded in 1973 and is headquartered in Paris, France.

113,496 Employees
Last Reported Date: 03/11/15
Founded in 1973

sanofi (SAN) Top Compensated Officers

No compensation data is available at this time for the top officers at this company.

Executives, Board Directors

sanofi (SAN) Key Developments

Lazard Reportedly Works With Sanofi On $12.7 Billion Animal Health Unit Deal

Lazard Ltd. (NYSE:LAZ) is reportedly working with Sanofi (ENXTPA:SAN)'s management in the listing of its Merial animal health unit for sale. Lazard is aiming to land the leading advisory job for the deal, sources familiar with the matter said. Sanofi and Lazard declined to comment.

Sanofi Reports Results of New Study Examining Perceptions of Risks Associated with Counterfeit Medicines

Sanofi reported the results of a new study examining perceptions of the risks associated with counterfeit medicines. Conducted in July 2015, the company said that the study sheds light on Americans' perceptions of counterfeit medicines. The findings show that only 12% of respondents feel that they have enough information on counterfeit medicines, and in most cases, are more likely to associate counterfeiting with consumer goods rather than medicines. Only 15% of American respondents made the connection between counterfeiting and medicines, while 54% linked the issue more with apparel and 43% with luxury goods. More than half of Americans (53%) said they had never heard of counterfeit medicines, and a vast majority (82%) felt that they had never been exposed to counterfeit drugs. 54% of Americans considered that the danger from counterfeit drugs was undisputable, while 40% felt that it was potential. 41% of respondents said they had no information about counterfeit medicines, and only 12% felt that they had been given sufficient information. Eight out of every 10 Americans feel that the greater risk of exposure to counterfeit drugs stems from the purchase of medicines online (79%). 62% feel that there is also a risk when traveling abroad. Yet they also believe it possible that counterfeit medicines might be found in traditional retail channels in the United States (59%). Only 18% of Americans had already purchased medicines online and three-quarters were not aware of the fact that there was a risk involved (74%) Purchasing Medicines Abroad: A Major Risk With typical foresight, 77% of all Americans travel with their own medicines, and almost 50% keep these products in their carry-on luggage whenever they fly (47%). As most of them feel that buying medicines abroad is a risky business, only 16% of US travelers actually do it, and 78% of them only buy from pharmacies. Under these conditions, 70% of Americans feel safe about buying, although this feeling of security varies according to destination: 83% when buying in Europe, but only 50% when purchases are made in Asia. Actively Committed to the Fight Against Counterfeit Medicines Sanofi has introduced three levels of protection for its medicines to defend the integrity and tamper-proof seal of each box, and to ensure product authentication and traceability. This level of precaution goes well beyond regulatory obligations. Sanofi set up a central coordination unit as early as 2007, assembling the internal centers of expertise that are potentially affected by fake drugs: Industrial Affairs, Safety, Medical and Regulatory Affairs, Legal, Public Affairs and Communication. This operational and territorial grid is conducive to greater responsiveness and allows the implementation of concrete actions in the fight against counterfeit medicines. In 2008, Sanofi created the Central Anti-Counterfeiting Laboratory (LCAC), located at a pharmaceutical site in the city of Tours to analyze suspected counterfeit products. Approximately 4,000 samples are sent to the laboratory each year from all over the world, forwarded by health authorities or seized by police or customs authorities. The company is also developing platforms designed to alert the general public by way of a website that aims to provide information and advice to raise vigilance over fake medicines and a mobile app for travelers called "travel tips." Lastly, Sanofi actively cooperates with national and international authorities to identify illicit platforms and to help take down illegal networks that threaten public health and safety with counterfeit medicines.

Sanofi and Regeneron Pharmaceuticals, Inc. Complete Enrollment in the Global Phase 3 ODYSSEY OUTCOMES Trial

Sanofi and Regeneron Pharmaceuticals, Inc. announced that the companies have completed enrollment in the global Phase 3 ODYSSEY OUTCOMES trial, which is prospectively evaluating the potential cardiovascular (CV) benefits of Praluent(R) (alirocumab) Injection after an acute coronary syndrome (ACS). The 18,000-patient ODYSSEY OUTCOMES trial is expected to be completed in 2017. ODYSSEY OUTCOMES is designed to determine whether the addition of Praluent to intensive statin therapy reduces major adverse cardiac events among patients who had previously experienced an ACS, such as a heart attack or unstable angina. The primary endpoint evaluates the time to first occurrence of coronary heart disease death, acute myocardial infarction, hospitalization for unstable angina, or fatal and non-fatal ischemic stroke. Patients with recent ACS were selected as the study population because they face a higher risk of recurrent events than patients with stable cardiovascular disease. Praluent is currently approved in the U.S. and EU to reduce bad (LDL) cholesterol in some patients with significant unmet need, including those with established cardiovascular disease, or an inherited form of high cholesterol, called heterozygous familial hypercholesterolemia (HeFH). The effect of Praluent on CV morbidity and mortality has not been determined. The global ODYSSEY program includes 16 Phase 3 trials conducted at more than 2,000 study centers, around the world, and once complete will evaluate more than 25,000 patients. Data from this program helped form one of the most comprehensive data sets ever used for the initial regulatory filing of a cholesterol-lowering therapy. In completed trials, Praluent reduced LDL cholesterol by up to an additional 62% versus placebo, and was generally well-tolerated with an acceptable safety profile. Do not use PRALUENT if allergic to alirocumab or to any of the ingredients in PRALUENT. Before start using PRALUENT, tell healthcare provider about all medical conditions, including allergies, and if pregnant or plan to become pregnant or if breastfeeding or plan to breastfeed. PRALUENT can cause serious side effects, including allergic reactions that can be severe and require treatment in a hospital. The most common side effects of PRALUENT include: redness, itching, swelling, or pain/tenderness at the injection site, symptoms of the common cold, and flu or flu-like symptoms.


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