Supernus Pharmaceuticals Announces Receipt of Paragraph IV ANDA Filings for Qelbree, Plans to Defend Patents

Reuters

05-29

<a href="https://laohu8.com/S/SUPN">Supernus Pharmaceuticals</a> Announces Receipt of Paragraph IV ANDA Filings for Qelbree, Plans to Defend Patents

Supernus Pharmaceuticals recently announced receiving Paragraph IV Notice Letters from third parties who have submitted Abbreviated New Drug Applications (ANDAs) for viloxazine extended-release capsules in 100, 150, and 200 mg doses. The company plans to rigorously defend its intellectual property rights regarding Qelbree, which is currently protected by six U.S. patents listed in the FDA's Orange Book. These patents are set to expire between September 2029 and April 2035.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Supernus Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9459552-en) on May 28, 2025, and is solely responsible for the information contained therein.

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The company plans to rigorously defend its intellectual property rights regarding Qelbree, which is currently protected by six U.S. patents listed in the FDA's <a href=\"https://laohu8.com/S/FNCTF\">Orange</a> Book. These patents are set to expire between September 2029 and April 2035.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Supernus Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9459552-en) on May 28, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":null,"symbol_name":null,"start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250528:nNDLm6sW1:1","article_id":"2539406012","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2539406012","pubTimestamp":1748462749,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Supernus Pharmaceuticals recently announced receiving Paragraph IV Notice Letters from third parties who have submitted Abbreviated New Drug Applications  for viloxazine extended-release capsules in 100, 150, and 200 mg doses. 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