by Julie Stewart | Apr 21, 2020 | News, Product Approvals
Lincolnshire, Ill., April 21, 2020 — Nexus Pharmaceuticals announced today it has received U.S. Food and Drug Administration (FDA) approval for its patent-pending New Drug Application (NDA) Emerphed, the first and only premixed ephedrine in a ready-to-use 50 mg/10 mL...
by Patrick Weeks | Feb 21, 2019 | News, Product Approvals
Lincolnshire, Ill., February 21, 2019 — Nexus Pharmaceuticals announced today it has received U.S. Food and Drug Administration (FDA) approval for Prochlorperazine Edisylate Injection, USP in 10mg/2mL vial. “The launch further expands our generic injectable portfolio...
by Patrick Weeks | Feb 14, 2019 | News, Product Approvals
Lincolnshire, Ill., February 14, 2019 — Nexus Pharmaceuticals announced today it has received U.S. Food and Drug Administration (FDA) approval for Dicyclomine Hydrochloride (HCl) Injection, USP in 20mg/2mL vial, the generic equivalent to Bentyl®. Dicyclomine HCl, USP,...
by Patrick Weeks | Jan 16, 2019 | News, Product Approvals
Lincolnshire, Ill., January 16, 2019 — Nexus Pharmaceuticals Inc. announced today the U.S. Food and Drug Administration (FDA) approval of Busulfan Injection, the company’s AP-rated therapeutic equivalent for Busulfex® 60 mg/10 mL (6 mg/1 mL). “The FDA approval of...
by Patrick Weeks | Nov 15, 2018 | News, Product Approvals
Vernon Hills, IL., Nov. 15th, 2018 – Nexus Pharmaceuticals announced today the immediate availability in the United States for Arsenic Trioxide Injection. Nexus Pharmaceuticals’ Arsenic Trioxide Injection is available as 10mg per 10mL vial for injection. The product...
by Patrick Weeks | Oct 19, 2017 | News, Product Approvals
Vernon Hills, Ill., Oct. 19, 2017 — Nexus Pharmaceuticals announced today the immediate availability in the United States of Procainamide HCL Injection, USP. Nexus Pharmaceuticals’ Procainamide HCL Injection, USP is available as a multi dose vial containing 1,000 mg...
