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Home > New FDA Approvals > 144 - Aimovig for migraine; lofexidine for opioid withdrawal; 3-D printing 510(k) clearance; Gottleib statement on branded drug companies blocking generics
Podcast: New FDA Approvals
Episode:

144 - Aimovig for migraine; lofexidine for opioid withdrawal; 3-D printing 510(k) clearance; Gottleib statement on branded drug companies blocking generics

Category: Science & Medicine
Duration: 00:10:24
Publish Date: 2018-05-18 16:00:00
Description:

May 18, 2018

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1:03 FDA approves novel preventive treatment for migraine https://www.prnewswire.com/news-releases/fda-approves-novel-preventive-treatment-for-migraine-300650782.html

2:44 FDA approves LUCEMYRA™ (lofexidine) after priority review for the management of opioid withdrawal symptoms https://www.prnewswire.com/news-releases/fda-approves-us-worldmeds-lucemyra-lofexidine-after-priority-review-for-the-management-of-opioid-withdrawal-symptoms-300649939.html https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm607884.htm

4:55 FDA clears patient specific 3D printed bone segments for the global extremities market

https://www.prnewswire.com/news-releases/additive-orthopaedics-announces-fda-clearance-of-their-patient-specific-3d-printed-bone-segments-for-the-global-extremities-market-300649830.html

5:45 Statement from FDA Commissioner Scott Gottlieb, M.D., on new agency efforts to shine light on situations where drug makers may be pursuing gaming tactics to delay generic competition

https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm607930.htm

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