The European Medicines Agency (EMEA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the granting of a marketing authorization for Twynsta (telmisartan/amlodipine), from independent German drug major Boehringer Ingelheim. The drug is intended for the treatment of essential hypertension. The review for Twynsta began on 23 September 2009 with an active review time of 210 days.
Positive opinion for generics
The Committee also adopted positive opinions recommending the granting of marketing authorizations for the following generic medicines:
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 2024 | Headless Content Management with Blaze