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Home / Health News / Zydus Cadila gets USFDA approval to sell medicine which prevents rejection in organ transplants

Zydus Cadila gets USFDA approval to sell medicine which prevents rejection in organ transplants

New Delhi, Jan 9 (PTI) Drug firm Zydus Cadila today said it has received approval from the US health regulator to sell Sirolimus Tablets, used to prevent rejection in organ transplantation, in the Am

By: Agencies   | | Updated: January 13, 2014 4:46 pm
Tags: Pharma  USFDA  Zydus Cadila  

Zydus Cadila USFDANew Delhi, Jan 9 (PTI) Drug firm Zydus Cadila today said it has received approval from the US health regulator to sell Sirolimus Tablets, used to prevent rejection in organ transplantation, in the American market with 180 days of marketing exclusivity. Also Read - World Drug Day: Dealing with drug addiction

“Zydus Cadila received the final approval from the US Food and Drug Administration (USFDA) to market Sirolimus tablets 0.5 mg with 180 days of marketing exclusivity,” the company said in a statement. Also Read - US FDA approves first digital pill with ingestible sensor



The Ahmedabad-based firm has also received USFDA approval to market Duloxetine delayed release capsules in different strengths of 20 mg, 30 mg and 60 mg, it added. Also Read - Focusing on IP to increase access to healthcare is narrow approach

As per the IMS data in 2013, the sales of Sirolimus 0.5 mg is estimated at USD 11.7 million and the total market for Sirolimus stood at around USD 203.8 million.

The sales for Duloxetine was estimated at USD 5.5 billion in 2013.

While Sirolimus tablets are immunosuppressant drugs used to prevent rejection in organ transplantation, Duloxetine delayed release capsules fall in the anti-depressants segment.

Published : January 10, 2014 8:53 am | Updated:January 13, 2014 4:46 pm
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