ZETA Pharmaceuticals has a long history of pharma consulting and importing bulk active and inactive ingredients for the U.S. market. In past years this included nutritionals. Since 2001, our emphasis has been OTC and prescription pharmaceutical markets. As a result, we offer a broad and more diversified range of APIs to human and veterinary dosage manufacturers.
Over the years our focus has been to offer a lower cost alternative to our customer’s existing sources. With this charter comes the responsibility to present manufacturers who meet CGMP and FDA standards. To facilitate this process we continue to retain the services of FDA consultants to monitor GMP submissions and to conduct pre-FDA inspections.
A number of our products are schedule III and IV controlled substances. We have the experience and are very familiar with the regulatory guidelines and have the necessary DEA permits and warehouse facilities to handle these products.