This study showed that intravenous sodium valproate has non-inferior efficacy to intravenous phenytoin as the first-line treatment of SE. The intravenous sodium valproate group had better outcomes in ...

The US Food and Drug Administration (US FDA) has given its approval to Lupin to market 100 mg dosage of extended phenytoin sodium capsules, the pharmaceutical company said in a press release. The anti ...

Details concerning the Phenytoin Sodium combination medication encompass its pricing as well as its availability in various forms, including tablets, capsules, syrups, creams, gels, ointments, liquids ...

Phenytoin sodium extended capsules is an anti-epileptic product and indicated for the control of seizures and prevention and treatment of seizures occurring during or following neurosurgery Aurobindo ...

Credit: Shutterstock. The product is a ready-to-dilute, room temperature stable formulation of fosphenytoin for IV injection, which allows for point-of-care storage. The Food and Drug Administration ...

Aurobindo Pharma Ltd has received the final approval from the US Food & Drug Administration (USFDA) to manufacture and market extended Phenytoin Sodium capsules USP, 100mg. The approved ANDA ...

Unichem Laboratories has received ANDA approval for its Extended Phenytoin Sodium Capsules USP, 100 mg from the United States Food and Drug Administration (USFDA) to market a generic version of ...

During the study period, there were 92 patients diagnosed as SE. Of those 37, 17 SE patients received intravenous phenytoin and 20 received intravenous sodium valproate as the first-line treatment.