
The shares of Cipla dropped nearly 2 percent to its day's high on January 13 after the US FDA granted its final approval to rival Aurobindo Pharma for a generic version of the GSK's Advair inhalers. Citi called the development a "marginal negative" for Cipla.
The shares of the pharma major dropped to a nine-month low of Rs 1,436.60 apiece, before recovering some losses to close at Rs 1,448 apiece.
Respirent Pharmaceuticals and Lannett have received final approval from the US Food and Drug Administration (FDA) for a generic version of Advair Diskus, which is a key respiratory drug used to treat patients suffering from asthma and chronic obstructive pulmonary disease.
Notably, Aurobindo Pharma in July last year had announced the acquisition of Lannett for $250 million. Citi Research said that the generic version will likely add $30 million to $40 million to the company's annual US revenues.
Cipla has been awaiting FDA's approval for its own generic version of Advair. While noting that FDA's approval to Lannett was a "marginal negative" for Cipla, the international firm sees the pharma major getting the approval in near-term.
It further sees Advair contributing $50 million to Cipla's US revenue in FY27.
Cipla shares have fallen more than 3 percent in the past five days, and over 4 percent in the past one month. This comes after the stock gained around 76 percent in the past five years.
The stock currently has a P/E ratio of 21.70, and a market capitalization of nearly Rs 1.17 lakh crore.
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