Cipla gains 3% post USFDA approval for its generic HIV drug

The stock up 3% at Rs 622 on the BSE in early morning trade and is 6.6% away from its 52-week high of Rs 663 touched on November 7, 2017.

SI Reporter  |  Mumbai 

Shares of were up 3% at Rs 622 per share on the in early morning trade after the company said that it has received approval from the US Food and Drug Administration (USFDA) to market Efavirenz tablets, used to treat HIV-1 infections in adults.

The stock of company is 6.6% away from its 52-week high of Rs 663 touched on November 7, 2017 on the

“The company has received final approval for its Abbreviated New Drug Application (ANDA) for 600mg from the United States Food and Drug Administration (USFDA),” said in a press release on Tuesday after market hours.

Cipla’s 600mg is AB-rated generic therapeutic equivalent version of Bristol-Myers Squibb Company’s, Sustiva. It is indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 infection in adults and in pediatric patients at least 3 months old and weighing at least 3.5 kg, it added.

According to IQVIA (IMS Health), Sustiva and its generic equivalents had US sales of approximately $105 million for the 12-month period ending April 2018. The product is available for shipping immediately, the company said.

At 09:28 am; was trading 2.6% higher at Rs 618 on the BSE, as compared to 0.3% rise in the S&P Sensex. A combined 2.08 million shares changed hands on the counter on the and BSE so far.


First Published: Wed, June 20 2018. 09:31 IST