Sun Pharma receives USFDA approval for Cerebyx

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New Delhi, Mar 19 (UNI) Sun Pharmaceutical Industries Ltd today said it has received the US Food and Drug Administration approval for the Abbreviated New Drug Application (ANDA) to market a generic version of Parke Davis's Cerebyx, fosphenytoin sodium injection.

Fosphenytoin sodium Injection has annual sales of about 15 million dollars in the US, a company statemet said.

Fosphenytoin sodium is used for the control of generalised convulsive status epilepticus as well as for prevention and treatment of seizures occurring during neurosurgery.


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