The US Food and Drug Administration has approved new labeling for Mifeprex (mifepristone), allowing the abortion drug to be used through 70 days of pregnancy rather than the previous 49 days.
USA-based Danco Laboratories announced that the regulator had approved changes which include revisions to the prescribing information, patient medication guide, patient agreement form and prescriber agreement form.
These revisions reflect what Danco calls the ‘most current clinical practices and safety and efficacy data for Mifeprex’.
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