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MUMBAI, Tuesday, January 27, 2015

USFDA revokes approval for Ranbaxy’s capsules

In more trouble for Ranbaxy Laboratories, the U.S. Food and Drug Administration (FDA) has revoked the Indian company’s 180-day exclusivity to market esomeprazole magnesium delayed release capsule... »
More on pharmaceutical AND: company information
NEW DELHI, Monday, January 26, 2015

Gilead expands hepatitis C licensing pacts with Indian firms

91 developing countries together account for 54 per cent of the total worldwide population of individuals infected with the hepatitis C virus. »
More on pharmaceutical AND: company information
NEW DELHI, Friday, January 23, 2015

USFDA issues import alert on Ratlam facility of Ipca Lab

The U.S. health regulator has issued import alert on drugs produced at the Ratlam facility of Ipca Laboratories in Madhya Pradesh, following which the company has suspended shipment of active phar... »
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