{"id":53799,"date":"2023-02-09T18:02:03","date_gmt":"2023-02-09T17:02:03","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/nexus-pharmaceuticals-inc-receives-fda-approval-for-tirofiban-hydrochloride-injection\/"},"modified":"2023-02-09T18:02:03","modified_gmt":"2023-02-09T17:02:03","slug":"nexus-pharmaceuticals-inc-receives-fda-approval-for-tirofiban-hydrochloride-injection","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/nexus-pharmaceuticals-inc-receives-fda-approval-for-tirofiban-hydrochloride-injection\/","title":{"rendered":"Nexus Pharmaceuticals Inc. Receives FDA Approval for Tirofiban Hydrochloride Injection"},"content":{"rendered":"<div>\n<p>LINCOLNSHIRE, Ill.&#8211;(BUSINESS WIRE)&#8211;<a href=\"https:\/\/twitter.com\/hashtag\/ANDA?src=hash\" target=\"_blank\" rel=\"noopener\">#ANDA<\/a>&#8211;Nexus Pharmaceuticals Inc. announced that it has received US Food and Drug Administration (FDA) approval for Tirofiban Hydrochloride Injection in 5mg\/100mL single-dose IV-bags. Tentative approval has been granted for concentrations of 12.5mg\/250mL single-dose IV-bags. It is an AP-rated generic to AGGRASTAT<sup>\u00ae<\/sup>\u00a5.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20230209005576\/en\/834934\/5\/NexusLogoFinal10.2.15_transparent.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20230209005576\/en\/834934\/21\/NexusLogoFinal10.2.15_transparent.jpg\"><\/a><\/p>\n<p>\n\u201cWe look forward to expanding our product range in the cardiovascular and IV solution space,\u201d said Usman Ahmed, President and CEO. \u201cBeing granted this approval is a milestone for us, but also for patients who want more transparency in the healthcare they receive. We eagerly anticipate bringing it to market in the coming months.\u201d\n<\/p>\n<p>\nNexus Pharmaceuticals\u2019 Tirofiban Hydrochloride for Injection will be available in cartons of sole single-dose IV bags.\n<\/p>\n<p>\n<b>About Tirofiban Hydrochloride for Injection<\/b>\n<\/p>\n<p>\nTirofiban Hydrochloride for Injection is indicated to reduce the rate of thrombotic cardiovascular events (combined endpoint of death, myocardial infarction, or refractory ischemia\/repeat cardiac procedure) in patients with non-ST elevation acute coronary syndrome.\n<\/p>\n<p>\nFor prescribing information, please see the following <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2F21078818.fs1.hubspotusercontent-na1.net%2Fhubfs%2F21078818%2FTirofiban%2520PI.pdf&amp;esheet=53313962&amp;newsitemid=20230209005576&amp;lan=en-US&amp;anchor=link&amp;index=1&amp;md5=9b08710079a82c34b8f6f4c688e43294\" rel=\"nofollow noopener\" shape=\"rect\">link<\/a>.\n<\/p>\n<p>\n<b>About Nexus Pharmaceuticals Inc.<\/b>\n<\/p>\n<p>\nNexus Pharmaceuticals Inc., a US-based healthcare company and certified diverse supplier, specializes in innovative processes to make difficult-to-manufacture specialty and generic drugs that are easier to use, less labor-intensive, and more streamlined in practice. Nexus ensures that its high-quality FDA-approved drugs fulfill a critical unmet medical need and delivers dependable life-saving treatment options when and where they\u2019re needed most. For more information about Nexus Pharmaceuticals and its state-of-the-art manufacturing facility in Wisconsin, visit <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.nexuspharma.net%2Fproject-tomorrow%2F&amp;esheet=53313962&amp;newsitemid=20230209005576&amp;lan=en-US&amp;anchor=https%3A%2F%2Fwww.nexuspharma.net%2Fproject-tomorrow%2F&amp;index=2&amp;md5=c452274e901cd7b6526c64f0345a2363\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.nexuspharma.net\/project-tomorrow\/<\/a>.\n<\/p>\n<p>\n\u00a5AGGRASTAT<sup>\u00ae<\/sup> is a registered trademark of Medicure Inc.\n<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nDeana Mndrucic<br \/>\n<br \/><a target=\"_blank\" href=\"m&#97;&#x69;&#x6c;t&#111;&#58;&#x64;&#x6d;n&#100;&#114;&#x75;&#x63;i&#99;&#x40;&#x6e;&#x65;x&#117;&#x73;&#x70;h&#97;&#114;&#x6d;&#x61;&#46;&#110;&#101;&#x74;\" rel=\"nofollow noopener\" shape=\"rect\">&#100;&#109;&#x6e;&#x64;&#114;&#117;&#x63;&#x69;&#99;&#64;&#x6e;&#x65;&#120;&#117;&#x73;&#x70;&#104;&#97;&#x72;&#x6d;&#97;&#46;&#x6e;&#x65;&#116;<\/a><br \/>847-996-3790\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>LINCOLNSHIRE, Ill.&#8211;(BUSINESS WIRE)&#8211;#ANDA&#8211;Nexus Pharmaceuticals Inc. announced that it has received US Food and Drug Administration (FDA) approval for Tirofiban Hydrochloride Injection in 5mg\/100mL single-dose IV-bags. Tentative approval has been granted for concentrations of 12.5mg\/250mL single-dose IV-bags. It is an AP-rated generic to AGGRASTAT\u00ae\u00a5. \u201cWe look forward to expanding our product range in the cardiovascular and &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/nexus-pharmaceuticals-inc-receives-fda-approval-for-tirofiban-hydrochloride-injection\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-53799","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Nexus Pharmaceuticals Inc. Receives FDA Approval for Tirofiban Hydrochloride Injection - Pharma Trend<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pharma-trend.com\/en\/nexus-pharmaceuticals-inc-receives-fda-approval-for-tirofiban-hydrochloride-injection\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nexus Pharmaceuticals Inc. Receives FDA Approval for Tirofiban Hydrochloride Injection - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"LINCOLNSHIRE, Ill.&#8211;(BUSINESS WIRE)&#8211;#ANDA&#8211;Nexus Pharmaceuticals Inc. announced that it has received US Food and Drug Administration (FDA) approval for Tirofiban Hydrochloride Injection in 5mg\/100mL single-dose IV-bags. Tentative approval has been granted for concentrations of 12.5mg\/250mL single-dose IV-bags. 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