According to the FDA and the FD&C (Federal Food, Drug, and Cosmetic) Act, the product is considered bioequivalent and therapeutically equivalent to the reference listed drug (RLD), Potassium Chloride for Injection Concentrate, USP, of Hospira, Inc. Furthermore, the FDA has granted CGT (competitive generic therapy) designation for the 10mL and 20mL presentations.

“This approval highlights Nexus’ commitment to stabilizing the domestic pharmaceutical supply chain,” said Usman Ahmed, President and CEO of Nexus. “Potassium Chloride for Injection Concentrate has been on the FDA’s drug shortage list for several years and we are very proud to alleviate this shortage with a product manufactured in the United States. This product represents our fourth approval this year with many more to come as we continue to expand our portfolio of critical need medications.”

Nexus Pharmaceuticals’ Potassium Chloride for Injection Concentrate, USP is expected to launch in the next few weeks and will be available in cartons of 25 vials.

About Potassium Chloride for Injection Concentrate, USP

Potassium Chloride Injection is a sterile, nonpyrogenic, highly concentrated, ready-to-use, solution of Potassium Chloride, USP in Water for Injection, USP for electrolyte replenishment in a single dose container for intravenous administration.

Potassium Chloride Injection is indicated in the treatment of potassium deficiency states when oral replacement is not feasible.

About Nexus Pharmaceuticals LLC

Nexus Pharmaceuticals LLC., a US-based healthcare company, 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’re needed most.

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