Mayne Pharma debuts $80M solid dose plant in North Carolina

pills
The company expects to introduce more than 20 products and double its manufacturing volumes at the Greenville site. (Pixabay)

Australia’s Mayne Pharma has opened its $80 million oral solid-dose manufacturing facility in Greenville, North Carolina.

Construction on the 126,000-square-foot plant began two years ago. The plant more than quadruples Mayne’s capacity to produce oral solid-dose products in the U.S. to well over 1 billion doses and will allow for the manufacture of potent compounds and modified-release bead/pellet products, the company said.

Mayne scooped up 42 products from Teva and Allergan in 2016 as those two companies were looking to offload assets as part of an effort to win antitrust clearance for Teva’s $40.5 billion buyout of Allergan’s generics business. Mayne, which said it was focusing on U.S. generics growth, also bought 37 marketed generics plus 5 that were, at the time, under review at the FDA.

Free Daily Newsletter

Like this story? Subscribe to FiercePharma!

Biopharma is a fast-growing world where big ideas come along daily. Our subscribers rely on FiercePharma as their must-read source for the latest news, analysis and data on drugs and the companies that make them. Sign up today to get pharma news and updates delivered to your inbox and read on the go.

“This new Greenville facility will greatly enhance our internal capacity and capability to support the mid- to long-term growth potential we see for our business and allows us to manufacture in the United States advanced drug delivery technologies that until today were only available in our Australian facility,” Scott Richards, Mayne’s chief executive, said in a statement. “The new plant will enable us to better control our supply chain, serve our customers better and reduce product costs.”

Richards added that in the next few years the company expects to introduce more than 20 products and double its manufacturing volumes at the Greenville site.

Suggested Articles

The FDA is allowing some drugmakers to exceed the level of risk from a probable cancer-causing impurity in losartan for six months.

CDMOs Cambrex and Ajinomoto Bio-Pharma Services upgraded manufacturing plants, Takeda scored an albumin approval via its Shire deal, and more.

The FDA hit United Exchange Corp. with a warning letter, citing the company for a number of “significant” violations with its quality control systems.