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Aurobindo Pharma rises on USFDA nod for anti-AIDS drug

The stock has outperformed the market by surging 24% in past four trading sessions after USFDA has lifted the import alert for Unit VI Cephalosporin facility.

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SI Reporter Mumbai
Last Updated : Apr 03 2013 | 1:49 PM IST
Aurobindo Pharma is trading higher by 3% to Rs 161 after the company said it has received tentative approval from the US Food & Drug Administration (USFDA) to manufacture and market anti-AIDS combination drug Efavirenz/ Emtricitabine and Tenofovir Disoproxil Fumarate Tablets.

“The company is one of the first generics firm to have received the tentative approval to manufacture and market its anti-AIDS combination drug Efavirenz / Emtricitabine and Tenofovir Disoproxil Fumarate Tablets, 600mg/200mg/300mg from the USFDA,” Aurobindo Pharma said in a BSE filing.

The drug is the generic equivalent of Gilead Sciences Inc’s Atripla® Tablets 600mg/200mg/300mg and falls under the Anti-Retroviral (ARV) segment, it added.

Meanwhile, the stock has outperformed the market by surging 24% in past four trading sessions on BSE after USFDA has lifted the import alert for Unit VI Cephalosporin facility, which allows company to resume the supply of 9 products to US market from the same unit. The benchmark Sensex has gained 1.5% during the same period.

The stock opened at Rs 157 and hit a high of Rs 163 on BSE. A combined 3.61 million shares have changed hands on the counter so far on BSE and NSE.
 

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First Published: Apr 03 2013 | 12:42 PM IST

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