Sun Pharma gets FDA approval for generic of Optivar
Moneylife Digital Team 22 June 2010

Sun Pharmaceutical Industries Ltd said it received an abbreviated new drug application (ANDA) approval from the US Food and Drug Administration (USFDA) to market a generic version of Optivar, azelastine ophthalmic solution, 0.05%, in the US.

This sterile azelastine hydrochloride ophthalmic solution is therapeutically equivalent to Optivar Ophthalmic Solution 0.05% from Medpointe Pharmaceuticals and has annual sales of about $50 million in the US.
Azelastine is used for the treatment of the itching of the eyes associated with allergic conjunctivitis.

On Tuesday, Sun Pharma shares ended 0.3% up at Rs1,758 on the Bombay Stock Exchange, while the benchmark Sensex closed 0.7% down at 17,749 points.

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