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Sanofi Aventis

Jan 06, 2016 at 11:38 | Source: PTI
In a BSE filing, Glenmark said it "has been granted tentative approval by the US Food & Drug Administration (USFDA) for its Dronedarone Tablets, 400 mg, the generic version of Multaq Tablet, 400 mg of Sanofi-Aventis US LLC."
Jan 06, 2016 at 11:18 | Source: Moneycontrol.com
Glenmark Pharmaceuticals Inc, USA has been granted tentative approval by the USFDA for its Dronedarone tablets, 400 mg, the generic version of Multaq tablets, 400 mg of Sanofi-Aventis US LLC.
Jan 06, 2016 at 10:59 | Source: Moneycontrol.com
The company has received an approval for its Dronedarone tablets, 400 mg, the generic version of Multaq tablets, 400 mg of Sanofi-Aventis US LLC.
Dec 08, 2015 at 15:09 | Source: Moneycontrol.com
"Unichem has received ANDA approval from the United States Food and Drug Administration (USFDA) for Irbesartan tablets USP 75 mg, 150 mg and 300 mg," the pharma company said in its filing. The drug is equivalent to Avapro tablets of Sanofi-aventis US LLC.
Nov 20, 2015 at 21:32 | Source: PTI
"The transaction has been completed on November 20, 2015, upon fulfillment of the conditions precedent and the company has received the entire sale consideration of Rs 1110 million from the purchaser," Sanofi India said in a BSE filing.
Oct 11, 2015 at 11:27 | Source: PTI
The government is likely to commission a study soon to assess the impact of foreign direct investment in existing pharmaceutical companies in view of concerns expressed on the issue by a Parliamentary panel.
Jul 21, 2015 at 20:31 | Source: PTI
Standalone total income from operations also rose to Rs 549.7 crore for the quarter ended June 30, 2015 as against Rs 505.8 crore for the same period year ago, Sanofi India said in a filing to the BSE.
Sep 23, 2013 at 09:56 | Source: Moneycontrol.com
Genzyme, a fully-owned subsidiary of drug major Sanofi-Aventis, alleged that the Indian drug maker infringed patents of its blockbuster cancer drug Mozobil on three counts.
Sep 22, 2013 at 13:58 | Source: PTI
In its petition filed in the District Court of Delaware, Genzyme alleged that DRL intimated though a letter that it had submitted an Abbreviated New Drug Application with US FDA seeking approval to engage in the commercial manufacture, importation, use, and sale of 20 mg/ml Plerixafor injection as a generic version of Mobozil drug.
Sep 16, 2013 at 15:54 | Source: Moneycontrol.com
Pharma major, Lupin, announced today that it has received final approval for its Zolpidem Tartrate Extended-release tablets USP, 6.25 mg and 12.5 mg from the United States Food and Drugs Administration (FDA) to market a generic version of Sanofi Aventis, US, LLCs (Sanofi) Ambien CR Extended-release tablets, 6.25 mg and 12.5 mg.
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Pharmaceuticals - Sector  

Source:VC Circle - The Sanofi-Aventis group acquired Shantha Biotechnics in 2009, followed by the acquisition of the nutrition biz of Universal Medicare in 2011. French pharmaceutical company Sanofi S.A.'s animal health division Merial is acquiring the animal health unit

5.29 PM Dec 22nd 2012

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Lupin  

Source:Business Standard - Lupin Pharmaceuticals has received approval for its Irbesartan tablets, used for treating hypertension, from US Food and Drugs Administration (USFDA). The tablets are available in 75-300 mg strengths and are the AB-rated generic equivalent of Sanofi Aventis`s Avapro

1.16 PM Oct 18th 2012

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Unichem Labs  

Source:Business Standard - Unichem Laboratories today said it has received American health regulator`s tentative approval to market generic version of Sanofi Aventis` Avapro tablets, a hypertension drug, in the US market. The company has received tentative approval from the United States Food

1.13 PM Oct 18th 2012

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Lupin  

Source:The Hindu BusinessLine - Mumbai, October 17: Pharma major Lupin today said its subsidiary, Lupin Pharmaceuticals, has received approval for its Irbesartan tablets from the US Food and Drugs Administration (FDA) to market a generic version of Sanofi Aventis’s Avapro tablets

5.18 PM Oct 17th 2012

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Lupin  

Source:Business Standard - Lupin Limited has moved higher by 2% at Rs 564 on the Bombay Stock Exchange after the company said that its subsidiary has received a final approval for its Irbesatan tablets from the United States Food and Drugs Administration (FDA) to market a generic version of Sanofi

4.57 PM Oct 17th 2012

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Sanofi India  

Karvy Stock Broking has come out with its report on pharma pricing policy. The research firm initial assessment is based on a 50 % price cut and a possible 80% price cut for products marked in Light Blue. The impact based on the above methodology shows a higher impact on Sanofi Aventis, GSK Pharma

3.32 PM Sep 28th 2012

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foreign firms acquired big Indian companies such as Ranbaxy by Daiichi Sankyo of Japan, Shanta Biotech by Sanofi Aventis of France and Piramal Health Care`s health unit by Abbott Laboratories of the US. While the finance ministry wants that only those cases involving FDI beyond 49 per cent in existing

5.20 PM Sep 19th 2012

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Aventis Pharma  

Source:Economic Times - Income tax authorities summoned the management of Hyderabad based Shanta Biotechnics in connection with an outstanding tax demand of Rs 1058 crores faced by French drug giant Sanofi Aventis, two people familiar with the development told ET NOW. ET NOW was the first

1.32 PM Jul 6th 2012

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Aurobindo Pharm  

News 18th May 2012 Dr Reddy`s Laboratories, Sun Pharma and Aurobindo Pharma received FDA nod to sell generic version of Sanofi Aventis` Plavix tablets in the US market Hyderabad: Pharmaceutical companies, Dr Reddy`s Laboratories, Sun Pharma and Aurobindo Pharma on Friday said they have received US

12.22 PM May 25th 2012

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Venus Remedies  

but at the same time provides enhanced safety to patient and para-medical staff, Chaudhary added. A semi-synthetic cytostatic taxane analogue, Docetaxel was initially developed by Sanofi-Aventis and is marketed under the brand name “Taxotere”. The molecule patent protection of Sanofi-Aventis has recently expired

12.19 PM Mar 25th 2012

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