The US Food and Drug Administration has granted Novartis marketingclearance for its oral suspension formulation of the anticonvulsive Trileptal (oxcarbazepine), for the treatment of epilepsy. The drug was previously approved in tablet form two years ago (Marketletter October 4, 1999), but patients who are mentally impaired can have difficulty swallowing medication in this form. The new lemon-flavored liquid provides the same effective seizure control as the tablets but in an easy-to-swallow formulation.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze