www.fdanews.com/articles/86422-preotact-approved-in-europe
PREOTACT APPROVED IN EUROPE
April 28, 2006
NPS Pharmaceuticals and its partner Nycomed have received market authorization from the European Medicines Evaluation Agency (EMEA) for Preotact (parathyroid hormone [rDNA origin] for injection).
Preotact is approved to treat postmenopausal women at risk of bone fractures from osteoporosis. The company plans to begin shipping the drug later this year.